U.S. patent application number 12/281419 was filed with the patent office on 2009-02-12 for highly air-permeable and water-resistance sheet, a highly air-permeable and water-resistance sheet composite and an absorbent article, and a method for anufacturing a highly air-permeable and water-resistance sheet and a method for manufacturing a highly air-permeable and water-resistance sheet comp.
Invention is credited to Akira Kawase, Migaku Suzuki.
Application Number | 20090042468 12/281419 |
Document ID | / |
Family ID | 38459139 |
Filed Date | 2009-02-12 |
United States Patent
Application |
20090042468 |
Kind Code |
A1 |
Suzuki; Migaku ; et
al. |
February 12, 2009 |
HIGHLY AIR-PERMEABLE AND WATER-RESISTANCE SHEET, A HIGHLY
AIR-PERMEABLE AND WATER-RESISTANCE SHEET COMPOSITE AND AN ABSORBENT
ARTICLE, AND A METHOD FOR ANUFACTURING A HIGHLY AIR-PERMEABLE AND
WATER-RESISTANCE SHEET AND A METHOD FOR MANUFACTURING A HIGHLY
AIR-PERMEABLE AND WATER-RESISTANCE SHEET COMPOSITE
Abstract
The present invention provides highly air-permeable and
water-resistance sheet and a highly air-permeable and
water-resistance sheet having both of highly air permeability and
water resistance, and an absorbent article comprising thereof. In
addition, the present invention provides a highly air-permeable and
water-resistance sheet and method for manufacturing a highly
air-permeable and water-resistance sheet composite wherein the
sheet and composite have such a property. In the highly
air-permeable and water-resistance sheet according to the present
invention: A highly air-permeable and water-resistance sheet
comprising a hydrophobic non-woven fabric layer having 100
mmH.sub.2O or more of water pressure resistance; and a fine
cellulose fiber layer layered on said hydrophobic non-woven fabric
layer, wherein a water repellant layer is layered on either surface
of said highly air-permeable and water-resistance sheet.
Inventors: |
Suzuki; Migaku; (Tokyo,
JP) ; Kawase; Akira; (Tokyo, JP) |
Correspondence
Address: |
FROMMER LAWRENCE & HAUG
745 FIFTH AVENUE- 10TH FL.
NEW YORK
NY
10151
US
|
Family ID: |
38459139 |
Appl. No.: |
12/281419 |
Filed: |
March 1, 2007 |
PCT Filed: |
March 1, 2007 |
PCT NO: |
PCT/JP2007/053914 |
371 Date: |
September 2, 2008 |
Current U.S.
Class: |
442/76 ;
427/322 |
Current CPC
Class: |
B32B 23/10 20130101;
Y10T 442/2164 20150401; Y10T 442/674 20150401; D04H 3/16 20130101;
Y10T 442/68 20150401; Y10T 442/66 20150401; Y10T 442/681 20150401;
Y10T 442/2139 20150401; Y10T 442/669 20150401; Y10T 442/2213
20150401; Y10T 442/696 20150401; Y10T 442/668 20150401 |
Class at
Publication: |
442/76 ;
427/322 |
International
Class: |
B32B 5/18 20060101
B32B005/18; B05D 3/00 20060101 B05D003/00 |
Foreign Application Data
Date |
Code |
Application Number |
Mar 2, 2006 |
JP |
2006-056507 |
Sep 28, 2006 |
JP |
2006-265880 |
Nov 28, 2006 |
JP |
2006-320884 |
Claims
1. A highly air-permeable and water-resistance sheet comprising a
hydrophobic non-woven fabric layer having 100 mmH2O or more of
water pressure resistance; and a fine cellulose fiber layer layered
on said hydrophobic non-woven fabric layer, wherein a water
repellant layer is layered on either surface of said highly
air-permeable and water-resistance sheet.
2. The highly air-permeable and water-resistance sheet according to
claim 1, wherein said non-woven fabric is spun melt non-woven
fabric made of polyolefins.
3. The highly air-permeable and water-resistance sheet according to
claim 1, wherein said non-woven fabric is melt blown non-woven
fabric.
4. The highly air-permeable and water-resistance sheet according to
claim 1, wherein said non-woven fabric is composite non-woven
fabric of spun bond and melt blown non-woven fabric.
5. The highly air-permeable and water-resistance sheet according to
claim 1, wherein said fine cellulose fiber constituting said fine
cellulose fiber layer has 0.3 mm or less of average fiber length
and has 15 mL/g or more of hydration capacity.
6. The highly air-permeable and water-resistance sheet according to
claim 1, wherein weight of said fine cellulose fiber layer is in
the range of 2 to 20 g/m2.
7. The highly air-permeable and water-resistance sheet according to
claim 1, wherein said water repellant layer is layered on both
surfaces of said highly air-permeable and water-resistance
sheet.
8. The highly air-permeable and water-resistance sheet according to
claim 1, wherein said water repellant layer comprises an olefinic
water repellent, a synthetic resin binder and a cross linker.
9. The highly air-permeable and water-resistance sheet according to
claim 8, wherein said synthetic resin binder is stylene butadiene
resin.
10. The highly air-permeable and water-resistance sheet according
to claim 8, wherein said cross linker is ammonia zirconium
carbonate.
11. The highly air-permeable and water-resistance sheet according
to claim 1, wherein said water repellant layer further comprises a
deodorizer.
12. The highly air-permeable and water-resistance sheet according
to claim 11, wherein said deodorizer is zeolite originated from
natural resources.
13. The highly air-permeable and water-resistance sheet according
to claim 1, wherein said highly air-permeable and water-resistance
sheet is subjected to heat press treatment.
14. The highly air-permeable and water-resistance sheet according
to claim 1, wherein said highly air-permeable and water-resistance
sheet is of heat treated so as to melt at least part of
compositions of said hydrophobic non-woven fabric layer.
15. A highly air-permeable and water-resistance sheet composite
comprising a hydrophobic non-woven fabric layer and having 100
mmH2O or more of water pressure resistance; a fine cellulose fiber
layer layered on said hydrophobic non-woven fabric layer; and a
water repellant layer layered on said fine cellulose fiber layer,
wherein said highly air-permeable and water-resistance sheet
composite comprises another non-woven fabric layered onto said
water repellant layer.
16. The highly air-permeable and water-resistance sheet composite
according to claim 15, comprising another fine cellulose fiber
layer between said water repellant layer and said another non-woven
fabric.
17. An absorbent article comprising a highly air-permeable and
water-resistance sheet as claimed in claim 1, and an absorbent body
layered on said highly air-permeable and water-resistance
sheet.
18. An absorbent article comprising a highly air-permeable and
water-resistance sheet composite as claimed in claim 15, and an
absorbent body layered on said highly air-permeable and
water-resistance sheet composite.
19. The absorbent article as claimed in claim 17, wherein said
absorbent body has regions containing SAP and not containing
SAP.
20. The absorbent article as claimed in claim 17, wherein said
absorbent body contains 50% or more of said SAP relative to the
weight of said absorbent body.
21. The absorbent article as claimed in claim 17, further
comprising a buffer sheet between said highly air-permeable and
water-resistance sheet and said absorbent body.
22. The absorbent article as claimed in claim 21, wherein said
buffer sheet is an apertured film.
23. The absorbent article as claimed in claim 21, wherein a ratio
of the surface area of said buffer sheet is assigned as "P" and the
surface area of said is highly air-permeable and water-resistance
sheet is assigned as "Q", a ratio of P/Q.times.100 is in the range
of 10% to 50%.
24. A method for manufacturing a highly air-permeable and
water-resistance sheet comprising the steps of: degassing a
hydrophobic non-woven fabric layer having 100 mmH2O or more of
water pressure resistance using a degassing medium containing
water; layering a fine cellulose fiber layer to said degassed
hydrophobic non-woven fabric layer; and layering a water repellant
layer to said fine cellulose fiber layer.
25. The method for manufacturing a highly air-permeable and
water-resistance sheet according to claim 24, wherein said
degassing medium contains a hydrophilic organic solvent or a
surface-activating agent.
26. The method for manufacturing a highly air-permeable and
water-resistance sheet according to claim 25, wherein said
hydrophilic organic solvent is ethanol.
27. The method for manufacturing a highly air-permeable and
water-resistance sheet according to claim 25, wherein said
surface-activating agent is selected from the group consisting of
an adduct of nonylphenol ethylene oxide and a dodecylbenzene
sulfonic acid and a mixture thereof.
28. The method for manufacturing a highly air-permeable and
water-resistance sheet according to claim 24, wherein said step of
layering a fine cellulose fiber layer is performed using a slurry
of the fine cellulose fiber in water.
29. The method for manufacturing a highly air-permeable and
water-resistance sheet according to claim 25, wherein said slurry
contains a surface-activating agent.
30. A method for manufacturing a highly air-permeable and
water-resistance sheet composite comprising the steps of degassing
a hydrophobic non-woven fabric layer having 100 mmH2O or more of
water pressure resistance using a degassing medium containing
water; layering a fine cellulose fiber layer to said degassed
hydrophobic non-woven fabric layer; layering a water repellant
layer to said fine cellulose fiber layer; and layering another
non-woven fabric layer onto said water repellant layer.
31. The method for manufacturing a highly air-permeable and
water-resistance sheet composite as claimed in claim 30, comprising
another step of layering a fine cellulose fiber layer on said water
repellant layer between said step of layering a water repellant
layer and said step of layering another non-woven fabric layer.
32. The method for manufacturing a highly air-permeable and
water-resistance sheet composite as claimed in claim 30, wherein
said step of layering another non-woven fabric layer is a step of
layering said fine cellulose fiber layer layered on said non-woven
fabric such that said fine cellulose fiber layer is in contact with
said water repellant layer.
33. The method for manufacturing a highly air-permeable and
water-resistance sheet composite as claimed in claim 30, wherein
said layer having a non-woven fabric is degassed using the
degassing medium.
Description
TECHNICAL ART
[0001] The present invention relates to a highly air-permeable and
water-resistance sheet and a highly air-permeable and
water-resistance sheet composite, and absorbent article comprising
thereof, and a method for manufacturing a highly air-permeable and
water-resistance sheet and a method for manufacturing a highly
air-permeable and water-resistance sheet composite. In particular,
the present invention relates to a highly air-permeable and
water-resistance sheet and a highly air-permeable and
water-resistance sheet composite having both of highly air
permeability and water resistance, and a method for manufacturing
thereof, and an absorbent article comprising thereof.
BACKGROUND ART
[0002] The air permeable sheet material in the art is provided to
have a micro porous structure by forming a hydrophobic film
comprising the phase separated layer containing the filler such as
BaSO.sub.4 and CaCO.sub.3 and heterogeneous polymer, by
micro-dispersing the easily extractable component and extracting
the component, or by forming micro continuous foamed structure.
[0003] Such films having micro porous structure has been used for
the backsheet of hygiene products such as disposable diaper and
sanitary napkin, or has been in heavy usage for waterproof material
for rainwear and sports wear by laminating it to nonwoven fabric,
woven fabric knitted fabric.
[0004] In addition, the sheet member having a selective
permeability is widely used for the hygiene products such as the
absorbent product including diaper, and mask shutting off the
microscopic particles such as dust, microorganism and pollen. Such
a member includes a material supporting activated carbon in the
powder form, activated carbon fiber and zeolite.
[0005] Generally, these sheet members require a profile in
dependent on its application. Such a profile includes, for example
in the absorbent products, air permeability and water resistance
along with retaining water absorbability in dependence on the
constituent element of the products. In addition, such a profile,
in the hygiene products such as mask, includes to have a profile
inhibiting the passage of the above-mentioned microscopic particle,
along with air permeability. In order to obtain such a profile, the
securement of water resistance and impermeability can be attained
to reduce the pore size of the sheet member. However, the reduction
of the pore side leads to the limitation of the air permeability
thereby hard to obtain the necessary profile for the
applications.
[0006] There is the so-called breathable backsheet as the sheet
member having air permeability. Many proposals for manufacturing
this backsheet have been made including the layered products of
microfiber web and the method utilizing the gel blocking. However,
one and only effective mean as commercially adapted is to use the
air permeable PE film as the backsheet. However, the ventilation
rate of the normal air permeable film is in the range of about 3.0
to 5.0 kg/24 hrm.sup.2 of MVTR (Moisture Vapor Transfer Ratio), in
accordance with ASTM E96-63F or E96-80B. Accordingly, it has to say
to provide not enough profile on the practical use.
[0007] That is, according to several researched for the stuffy of
underwear and the others, 2 mm or more of gap between the underwear
surface and the skin surface will be necessary for generating the
surface airflow due to the bellows effect to inhibit to being
stuffy, along with high air permeability. In case of the normal
underwear, 1.0 sec/100 mL of air permeability of the underwear
expressed as Gurley method (JIS P8117) is possessed. In comparison
with the air permeable film, the normal underwear has 1
kg/minm.sup.2 or more of ventilation rate expressed in accordance
with ASTM D-737, the thin-type underwear has 10 kg/minm.sup.2 or
more of ventilation rate, and the wetted underwear has at least 0.5
kg/minm.sup.2 or more of moisture vapor transfer ratio. These
ventilation rates correspond to about 300 times of a ventilation
rate of the above-mentioned conventional air permeable film.
Therefore, the conventional air permeable film is not enough for
inhibiting the generation of being stuffy and rash.
[0008] The present inventors considers that a necessary air
permeability for an absorbent product such as diaper is at least
100 sec/100 mL of air permeability as expressed in accordance with
the Gurley method, preferably tens seconds/100 mL or lower of air
permeability. In addition, there is little gap for providing the
bellows effect in the current absorbent product such as diaper,
since the absorbent product is defined to closely contact with the
body as possible without any gaps. Accordingly, there is little
surface airflow of the product. Furthermore, a small air
permeability of the air permeable film is no help in the product
after the body fluid has adsorbed in the absorbent, since the
absorbent comprises itself a thick layer of pulp/SAP. It is
naturally that, in case of wearing the absorbent product being in
such state, the humidity and temperature within the product will be
increased and the product will be stuffy and rash will be
occurred.
[0009] In addition, there are several proposals that any
ventilation holes are provided in the side, front, rear and end of
the product although a risk of occurring any leakages from the
product is recognized. However, there is occurred a new problem
that excretions and smells originated from the excretions are
leaked through the ventilation hole.
[0010] That is, in order to be capable of manufacturing an
absorbent product which has highly air permeability and that there
is less chance to occur stuffy and rash, it is necessary to improve
air permeability of the backsheet, and further to provide stable
air permeable structure in the absorbent.
Patent-related Document 1
[0011] Japanese Patent Application Publication No. 248872/1998
Patent-related Document 2
[0012] WO2002/090106
Patent-related Document 3
[0013] Japanese Patent Application Publication No. 284090/1996
Patent-related Document 4
[0014] WO2004/009902
Patent-related Document 5
[0015] Japanese Patent Application Publication No. 168230/1998
Patent-related Document 6
[0016] Japanese Patent Application Publication No. 2000-201975
Non-Patent-related Document 1
[0017] Bioscience and Industry, vol. 50, No. 6, p. 534 (1992)
Non-Patent-related Document 2
[0018] JAPAN TAPPI Journal, vol. 53, No. 5, p. 91 (1999)
DISCLOSURE OF INVENTION
Problem to be Solved
[0019] The present invention is aimed to make in consideration of
the above-mentioned problem. That is, the present invention is to
provide highly air-permeable and water-resistance sheet and a
highly air-permeable and water-resistance sheet having both of
highly air permeability and water resistance, and an absorbent
article comprising thereof. In addition, the present invention is
to provide a highly air-permeable and water-resistance sheet and
method for manufacturing a highly air-permeable and
water-resistance sheet composite wherein the sheet and composite
have such a property.
Means for Solving the Problem
[0020] The highly air-permeable and water-resistance sheet
according to the present invention is characterized as follows:
[0021] A highly air-permeable and water-resistance sheet comprising
a hydrophobic non-woven fabric layer having 100 mmH.sub.2O or more
of water pressure resistance; and a fine cellulose fiber layer
layered on said hydrophobic non-woven fabric layer,
[0022] wherein a water repellant layer is layered on either surface
of said highly air-permeable and water-resistance sheet. Thereby,
both of air permeability and water resistance is obtained, and an
applicably useful highly air-permeable and water-resistance sheet
is obtained.
[0023] In the highly air-permeable and water-resistance sheet
according to the present invention, highly air-permeable and
water-resistance sheet, said non-woven fabric is spun melt
non-woven fabric made of polyolefins. Thereby, in addition to
advantageously ensuring the hydrophobicity, the cost is advantage,
since the spun melt made of polyolefins is inexpensive and easily
available with large amount.
[0024] In the highly air-permeable and water-resistance sheet
according to the present invention, said non-woven fabric is melt
blown non-woven fabric. Thereby, the hydrophobicity is
advantageously ensured, due to utilizing the nature of the micro
fiber originated from the melt blown non-woven fabric.
[0025] In the highly air-permeable and water-resistance sheet
according to the present invention, said non-woven fabric is
composite non-woven fabric of spun bond and melt blown non-woven
fabric. Thereby, the sheet can have a dense porous tissue and can
maintain the stable water resistance property by means of the
structure combined the filament tissue of the spun bond non-woven
fabric with the micro tissue of the melt blown.
[0026] In the highly air-permeable and water-resistance sheet
according to the present invention, said fine cellulose fiber
constituting said fine cellulose fiber layer has 0.3 mm or less of
average fiber length and has 15 mL/g or more of hydration capacity.
Thereby, in addition to obtaining the fill-up effect to incorporate
the cellulose fiber into the porous portion of the fiber of the
hydrophobic non-woven fabric, the layer delamination between the
fine cellulose fiber layer and the hydrophobic non-woven fabric
layer can be prevented.
[0027] In the highly air-permeable and water-resistance sheet
according to the present invention, weight of said fine cellulose
fiber layer is in the range of 2 to 20 g/m.sup.2. Thereby, in
addition to securing the flexibility, the crack of the fine
cellulose fiber layer can be prevented.
[0028] In the highly air-permeable and water-resistance sheet
according to the present invention, said water repellant layer is
layered on both surfaces of said highly air-permeable and
water-resistance sheet. Thereby, the stable water resistance can be
enhanced.
[0029] In the highly air-permeable and water-resistance sheet
according to the present invention, said water repellant layer
comprises an olefinic water repellent, a synthetic resin binder and
a cross linker. Thereby, effects of each component constituting the
water repellant layer can be continuously sustained.
[0030] In the highly air-permeable and water-resistance sheet
according to the present invention, said synthetic resin binder is
stylene butadiene resin. Thereby, the water resistance due to the
film forming and the compatibility to the water repellant can be
improved, and the above-mentioned effects can be remarkably
obtained.
[0031] In the highly air-permeable and water-resistance sheet
according to the present invention, said cross linker is ammonia
zirconium carbonate. Thereby, the water resistance and the
sustained effect of the water repellant can be obtained, and it is
possible to prevent the water leakage for long time.
[0032] In the highly air-permeable and water-resistance sheet
according to the present invention, said water repellant layer
further comprises a deodorizer. Thereby, in addition to maintaining
the water resistance and the water repellency, it is possible to
obtain the deodorant effect.
[0033] In the highly air-permeable and water-resistance sheet
according to the present invention, said deodorizer is zeolite
originated from natural resources. Thereby, the appearance is
superior, and the deodorant effect can be obtained, along with the
reduction of the cost.
[0034] In the highly air-permeable and water-resistance sheet
according to the present invention, said highly air-permeable and
water-resistance sheet is subjected to heat press treatment.
Thereby, in addition to increasing the mechanical strength, the
highly air-permeable and water-resistance sheet having high
smoothness can be obtained.
[0035] In the highly air-permeable and water-resistance sheet
according to the present invention, said highly air-permeable and
water-resistance sheet is of heat treated so as to melt at least
part of compositions of said hydrophobic non-woven fabric layer.
Thereby, the fine cellulose fiber layer and the hydrophobic
non-woven fabric layer can be more integrated and can be smaller
and lighter.
[0036] In addition, the highly air-permeable and water-resistance
sheet composite according to the present invention is characterized
as follows:
[0037] A highly air-permeable and water-resistance sheet composite
comprising a hydrophobic non-woven fabric layer and having 100
mmH.sub.2O or more of water pressure resistance; a fine cellulose
fiber layer layered on said hydrophobic non-woven fabric layer; and
a water repellant layer layered on said fine cellulose fiber
layer,
[0038] wherein said highly air-permeable and water-resistance sheet
composite comprises another non-woven fabric layered onto said
water repellant layer. Thereby, in addition to improving the air
permeability, the water resistant and the surface
abrasion-resistant, the applicably useful highly air-permeable and
water-resistance sheet composite can be obtained wherein the dust
created from the surface can be prevented, and the passage of the
fine component such as microorganism and the dust can be
prevented.
[0039] In the highly air-permeable and water-resistance sheet
composite according to the present invention, it comprises another
fine cellulose fiber layer between said water repellant layer and
said another non-woven fabric. Thereby, the composite body having
two efficiencies of the water repellency and the moisture
absorbability can be obtained.
[0040] In addition, the absorbent article according to the present
invention is characterized as follows: An absorbent article
comprising a highly air-permeable and water-resistance sheet as
claimed in any one of Claims 1 to 14, and an absorbent body layered
on said highly air-permeable and water-resistance sheet. In
addition, the absorbent article according to the present invention
is characterized as follows:
[0041] An absorbent article comprising a highly air-permeable and
water-resistance sheet composite as claimed in Claim 15 or 16, and
an absorbent body layered on said highly air-permeable and
water-resistance sheet composite. Thereby, the absorbent article
can be obtained wherein it does not occur any leakage and be stuffy
along with having the absorbability of the liquid such as body
fluid.
[0042] In the absorbent article according to the present invention,
said absorbent body has regions containing SAP and not containing
SAP. Thereby, it is possible to ensure the good air permeability
even after the liquid such as the body liquid has absorbed.
[0043] In the absorbent article according to the present invention,
said absorbent body contains 50% or more of said SAP relative to
the weight of said absorbent body. Thereby, the cost is superior,
and enough air permeability can be obtained along with ensuring the
enough absorbability.
[0044] In the absorbent article according to the present invention,
it further comprises a buffer sheet between said highly
air-permeable and water-resistance sheet and said absorbent body.
Thereby, it is possible to ensure the stable water resistant for
long time even under the load.
[0045] In the absorbent article according to the present invention,
said buffer sheet is an apertured film. Thereby, the effect of the
buffer sheet can be obtained along with maintaining the high air
permeability.
[0046] In the absorbent article according to the present invention,
a ratio of the surface area of said buffer sheet is assigned as "P"
and the surface area of said is highly air-permeable and
water-resistance sheet is assigned as "Q", a ratio of P/Q.times.100
is in the range of 10% to 50%. Thereby, the cost is superior, and
it is possible to maintain enough air permeability and water
resistant.
[0047] On the other hand, the method for manufacturing a highly
air-permeable and water-resistance sheet according to the present
invention is characterized as follows:
[0048] A method for manufacturing a highly air-permeable and
water-resistance sheet comprising the steps of:
[0049] degassing a hydrophobic non-woven fabric layer having 100
mmH.sub.2O or more of water pressure resistance using a degassing
medium containing water;
[0050] layering a fine cellulose fiber layer to said degassed
hydrophobic non-woven fabric layer; and
[0051] layering a water repellant layer to said fine cellulose
fiber layer. Thereby, the highly air-permeable and water-resistance
sheet can be obtained with the convenient method by hydrophobizing
the fine cellulose fiber layer.
[0052] In the method for manufacturing a highly air-permeable and
water-resistance sheet according to the present invention, said
degassing medium contains a hydrophilic organic solvent or a
surface-activating agent. Thereby, it is possible to uniformly
layer the hydrophilic fine cellulose fiber layer on the hydrophobic
non-woven fabric layer.
[0053] In the method for manufacturing a highly air-permeable and
water-resistance sheet according to the present invention, said
hydrophilic organic solvent is ethanol. Thereby, independent of the
nature of the material such as hydrophilicity and hydrophobicity,
it is possible to uniformly layer the fine cellulose fiber
layer.
[0054] In the method for manufacturing a highly air-permeable and
water-resistance sheet according to the present invention, said
surface-activating agent is selected from the group consisting of
an adduct of nonylphenol ethylene oxide and a dodecylbenzene
sulfonic acid and a mixture thereof. Thereby, it is possible to
uniformly layer the fine cellulose fiber layer on the surface of
the hydrophobic non-woven fabric layer.
[0055] In the method for manufacturing a highly air-permeable and
water-resistance sheet according to the present invention, said
step of layering a fine cellulose fiber layer is performed using a
slurry of the fine cellulose fiber in water. Thereby, it is
possible to conveniently provide the function of the fine cellulose
fiber layer, without any facilities such as for recovering the
waste containing the solvent.
[0056] In the method for manufacturing a highly air-permeable and
water-resistance sheet according to the present invention, said
slurry contains a surface-activating agent. Thereby, it is possible
to uniformly layer the fine cellulose fiber layer on the surface of
the hydrophobic non-woven fabric.
[0057] In addition, the method for manufacturing a highly
air-permeable and water-resistance sheet composite according to the
present invention is characterized as follows:
[0058] A method for manufacturing a highly air-permeable and
water-resistance sheet composite comprising the steps of
[0059] degassing a hydrophobic non-woven fabric layer having 100
mmH.sub.2O or more of water pressure resistance using a degassing
medium containing water;
[0060] layering a fine cellulose fiber layer to said degassed
hydrophobic non-woven fabric layer;
[0061] layering a water repellant layer to said fine cellulose
fiber layer; and
[0062] layering another non-woven fabric layer onto said water
repellant layer. Thereby, the surface abrasion-resistance can be
enhanced, the desorption of the fine cellulose fiber from the
surface can be prevented, the dust created from the surface of the
highly air-permeable and water-resistance sheet composite can be
prevented.
[0063] In the method for manufacturing a highly air-permeable and
water-resistance sheet composite according to the present
invention, it comprises another step of layering a fine cellulose
fiber layer on said water repellant layer between said step of
layering a water repellant layer and said step of layering another
non-woven fabric layer. Thereby, it is possible to easily
manufacture the highly air-permeable and water-resistance sheet
composite which has different properties of water resistant and the
hydrophilicity.
[0064] In the method for manufacturing a highly air-permeable and
water-resistance sheet composite according to the present
invention, said step of layering another non-woven fabric layer is
a step of layering said fine cellulose fiber layer layered on said
non-woven fabric such that said fine cellulose fiber layer is in
contact with said water repellant layer. Thereby, the composite
body has both natures of water resistant and the hydrophilicity,
and the surface abrasion-resistance can be enhanced by covering the
surface of the fine cellulose fiber layer with the non-woven
fabric.
[0065] In the method for manufacturing a highly air-permeable and
water-resistance sheet composite according to the present
invention, said layer having a non-woven fabric is degassed using
the degassing medium. Thereby, it is possible to prevent to create
the uneven portion such as blistering phenomenon with partially
containing the air, and to continuously perform the uniform
coating.
EFFECT OF INVENTION
[0066] According to the present invention, both of water resistance
and air permeability can be obtained. In addition, it is possible
to prevent a passage of fine components such as microorganisms and
dust, in addition to water resistance and air permeability.
Further, it is possible to obtain properties originated from
several members by positioning materials having different
properties at predetermined position, without loss of the original
characteristics of highly air permeability and water
resistance.
BRIEF EXPLANATION OF DRAWING
[0067] FIG. 1a is a schematic cross-section view of the highly
air-permeable and water-resistance sheet according to the present
invention;
[0068] FIG. 1b is a schematic cross-section view of the highly
air-permeable and water-resistance sheet according to the present
invention;
[0069] FIG. 2a is a schematic cross-section view of the highly
air-permeable and water-resistance sheet according to the present
invention;
[0070] FIG. 2b is a schematic cross-section view of the highly
air-permeable and water-resistance sheet according to the present
invention;
[0071] FIG. 3A is a flowchart showing a method for manufacturing
the highly air-permeable and water-resistance sheet according to
the present invention;
[0072] FIG. 3B is a flowchart showing a method for manufacturing
the highly air-permeable and water-resistance sheet according to
the present invention;
[0073] FIG. 3C is a flowchart showing a method for manufacturing
the highly air-permeable and water-resistance sheet according to
the present invention;
[0074] FIG. 3D is a flowchart showing a method for manufacturing
the highly air-permeable and water-resistance sheet according to
the present invention;
[0075] FIG. 3E is a flowchart showing a method for manufacturing
the highly air-permeable and water-resistance sheet according to
the present invention;
[0076] FIG. 4A is a schematic view of the coating unit in the
apparatus for manufacturing the highly air-permeable and
water-resistance sheet according to the present invention;
[0077] FIG. 4B is an enlarged view of FIG. 4A;
[0078] FIG. 5A is one of aspects of the apparatus for manufacturing
the highly air-permeable and water-resistance sheet according to
the present invention;
[0079] FIG. 5B is a plan view of FIG. 5A taken in the direction
X-X';
[0080] FIG. 5C is a plan view of FIG. 5A taken in the direction
Y-Y';
[0081] FIG. 6 is one of aspects of the apparatus for manufacturing
the highly air-permeable and water-resistance sheet according to
the present invention;
[0082] FIG. 7 is a partial schematic cross section view of the
absorbent article according to one aspect of the present
invention;
[0083] FIG. 8 is a partial schematic cross section view of the
absorbent article according to another aspect of the present
invention;
[0084] FIG. 9 is a partial schematic cross section view of the
absorbent article according to the present invention further
comprising an apertured film;
[0085] FIG. 10 is views showing one aspects of absorbent body in
the sheet form used for the absorbent article according to the
present invention, wherein (a), (c) and (d) indicate plan views
thereof and (b) indicates the cross-sectional view of (a);
[0086] FIG. 11 is a schematic view showing one of examples of the
apertured film in the present invention;
[0087] FIG. 12 is a deployed plan view of a disposable diaper, one
of examples of the absorbent article according to the present
invention;
[0088] FIG. 13 is a cross-sectional view of FIG. 12 taken in line
A-B;
[0089] FIG. 14A shows a development view of the absorbent article
according to one of aspects of the present invention;
[0090] FIG. 14B is a cross-sectional view of FIG. 14A along with
line X-X';
[0091] FIG. 14C is a cross-sectional view of FIG. 14A along with
line Y-Y';
[0092] FIG. 14D is a schematic diagram of the absorbent article
according to one aspect of the present invention;
[0093] FIG. 15A is a schematic plan view showing one aspect of the
absorbent body in the present invention;
[0094] FIG. 15B is a schematic cross-sectional view showing one
aspect of the absorbent body in the present invention;
[0095] FIG. 16 is a schematic view showing one aspect of the
absorbent article according to the present invention;
[0096] FIG. 17 is a schematic view showing one aspect of the
absorbent article according to the present invention;
[0097] FIG. 18 shows a schematic view of an apparatus for examining
water resistance, wherein (a) indicates an overall view thereof,
and (b) indicates an enlarged view of the sample applied portion in
the apparatus;
[0098] FIG. 19 is a pattern diagram of an apparatus for confirming
the deodorizing efficiency using ammonium; and
[0099] FIG. 20 is a pattern diagram of an apparatus for confirming
the deodorizing efficiency using ammonium.
EXPLANATION OF NOTATION
[0100] 10 highly air-permeable and water-resistance sheet [0101] 12
fine cellulose fiber layer [0102] 13 water repellant layer [0103]
14 hydrophobic non-woven fabric layer [0104] 15 non-woven fabric
layer [0105] 16 absorbent body [0106] 18 apertured film [0107] 20
highly air-permeable and water-resistance sheet composite [0108] 22
fine cellulose fiber layer [0109] 23 water repellant layer [0110]
24 hydrophobic non-woven fabric layer [0111] 100 absorbent article
[0112] 110 leakage preventing material [0113] 112 first leakage
preventing body [0114] 114 second leakage preventing body [0115]
116 absorbent body [0116] 122 top sheet [0117] 124 bridge member
[0118] 126 urine-feces stopper [0119] 128 leg gather [0120] 130 leg
gather [0121] 132 connecting part [0122] 134 slit [0123] 136
projecting part [0124] 142 connecting part [0125] 144 connected
part [0126] 200 sheet [0127] 202 coating slurry [0128] 204
saturation medium [0129] 206 saturation medium layer [0130] 210 net
conveyer [0131] 212 head box [0132] 214 saturation medium supplier
[0133] 220 coating roller [0134] 222 roller [0135] 224 supporting
roller [0136] 232 unreeler [0137] 234 vacuum unit [0138] 236 plate
[0139] 238 tray [0140] 242 coating region [0141] 244 water stream
[0142] 301 jack [0143] 302 glass plate [0144] 303 filter paper
[0145] 304 sample [0146] 305 tissue paper [0147] 306 acrylic pipe
[0148] 307 acrylic mounter [0149] 308 packing [0150] 309 stand
[0151] 310 clamp [0152] 312 funnel [0153] 313 mirror [0154] A A
surface [0155] B B surface [0156] LH leg hole [0157] P urine
receiving part [0158] Q feces receiving part [0159] W waist hole
[0160] X direction [0161] Y direction
BEST MODE FOR CARRYING OUT THE PRESENT INVENTION
[0162] Hereinafter, preferred embodiments of the present invention
are explained.
[0163] <The Highly Air-Permeable and Water-Resistance Sheet
According to the Present Invention>
[0164] With reference to the Drawing, the highly air-permeable and
water-resistance sheet according to the present invention is
explained. It should be noted that the similar notation number adds
for the similar member, and that a member added same notation
number refers to the similar member, as long as specifically not
notifying.
[0165] The FIGS. 1a and 1b show a schematic cross-section view of
the highly air-permeable and water-resistance sheet according to
the present invention. According to FIGS. 1a and 1b, the highly
air-permeable and water-resistance sheet according to the present
invention comprises a hydrophobic non-woven fabric layer 14
consisting of a non-woven fabric and having 100 mmH.sub.2O or more
of water pressure resistance and a fine cellulose fiber layer 12
layered on the hydrophobic non-woven fabric layer 14 (hereinafter,
a member comprising the fine cellulose fiber layer 12 and the
hydrophobic non-woven fabric layer 14 also refers to as "composite
sheet"). In the highly air-permeable and water-resistance sheet
according to the present invention, a water repellant layer 13 is
layered on either or both of the surface of the composite sheet
(hereinafter, the layering the water repellant layer also refers to
as "water repellant treatment"). It should be noted that although
FIGS. 1a and 1b show the highly air-permeable and water-resistance
sheet comprising the water repellant layer 13 layered on the fine
cellulose fiber layer 12, in the highly air-permeable and
water-resistance sheet according to the present invention, the
water repellant layer 13 may be layered such that it is only
contact with the hydrophobic non-woven fabric layer 14 (on the
lower side surface of the Figure), or may be layered on both
surfaces thereof.
[0166] In both of the highly air-permeable and water-resistance
sheet as shown in FIGS. 1a and 1b, the fine cellulose fiber layer
and the hydrophobic non-woven fabric layer are layered each other.
The difference between FIGS. 1a and 1b is that the fine cellulose
fiber layer 12 is merely layered on the hydrophobic non-woven
fabric layer 14 in the highly air-permeable and water-resistance
sheet as shown FIG. 1a, while the fine cellulose fiber layer 12 is
positioned within the hydrophobic non-woven fabric layer 14 to fill
up the void of the hydrophobic non-woven fabric layer with the fine
cellulose fiber layer. In consideration of the lamination between
the layers, the highly air-permeable and water-resistance sheet
according to the present invention is preferable an aspect of
showing FIG. 1b. It should be noted that the water repellant layer
acts such that it is not covered on the surface of the fine
cellulose fiber layer to form the film of the water repellant
layer, and such that most of the water repellant layer is
penetrated into the fine cellulose fiber layer to cover each
surface of the fine cellulose fiber, thereby imparting
hydrophobicity by repelling effect to hydrophilicity.
[0167] The highly air-permeable and water-resistance sheet
according to the present invention mainly comprises three
components of the hydrophobic non-woven fabric layer, the fine
cellulose fiber layer consisting of e.g. micro fibrillated
cellulose (MFC), and the water repellant layer. In order to
manufacture the highly air-permeable and water-resistance sheet
comprising these three components, it is necessary to firstly
constitute a hydrophobic non-woven fabric layer/fine cellulose
fiber layer wherein the second component of the fine cellulose
fiber layer (e.g. MFC) is layered on the first component of the
hydrophobic non-woven fabric layer (hereinafter, also referred to
as "substrate") to constitute the hydrophobic non-woven fabric
layer/fine cellulose fiber layer. Further, the surface of the
hydrophobic non-woven fabric layer/fine cellulose fiber layer is
subjected to water repellent treatment with the third component of
the water repellant layer to obtain the highly air-permeable and
water-resistance sheet according to the present invention. It
should be noted that any additives such as synthetic resin for
reinforcement, color pigment and deodorant may be contained in the
water repellent treatment agent, and that the surface of the sheet
may be treated with printing materials. First, the hydrophobic
non-woven fabric layer and the fine cellulose fiber layer will be
explained.
[0168] (The Hydrophobic Non-Woven Fabric Layer)
[0169] In the highly air-permeable and water-resistance sheet
according to the present invention, the material and constitution
of the hydrophobic non-woven fabric layer is not limited so far as
it consists of the non-woven fabric and has 100 mmH.sub.2O or more
of water pressure resistance. The non-woven fabric used in the
present invention may be manufactured from several materials
including natural fibers such as wool and cotton, chemical fibers
such as rayon and acetate, synthetic fibers, and inorganic fibers
such as glass fibers and carbon fibers. In particular, the
non-woven fabric is desirable that it is porous, has less
wettability and a predetermined resistance of permeability to water
and has thin and uniformity as possible. For example, the
hydrophobic non-woven fabric layer includes non-woven fabric
consisting of so-called chemical synthetic fibers including resins
like as PE, PP, PET, nylon, PVA, acetate and polyurethane. For
example, it includes PE fiber, PP fiber, PET fiber, nylon fiber,
PVA fiber, acetate fiber, PE/PP composite fiber, PE/PET composite
fiber, and PET derivatives/PET composite fiber. In addition, it may
include the spun bonded non-woven fabric and the melt blown
non-woven fabric wherein the spun bonded non-woven fabric and the
melt blown non-woven fabric are of being directly non-woven in
accordance with the spun melt method, respectively. In addition,
the non-woven fabric may be a non-woven fabric formed from the
fibrillated fibers by the spray spinning, and a non-woven sheet
pressed with continuous highly foamed body. Among them, spun melt
non-woven fabric made of polyolefins is preferable.
[0170] The spun melt non-woven fabric may be manufactured from a
non-woven fabric made by the spun bonded (S), and a non-woven
fabric made by the melt blown (M) to form SMS (spun bond/melt
blown/spun bond) non-woven fabric, SMMS (spun bond/melt blown/melt
blown/spun bond) non-woven fabric and SMSM non-woven fabric.
[0171] In the non-woven fabric made from the spun bonded (S) and
the melt blown (M), the M/S ratio of the non-woven fabric made from
spun bonded (S) and the melt blown (M) may be appropriately
selected in accordance with dense property to be needed including
pore size and water pressure resistance of the non-woven fabric.
For example, the weight ratio of spun bond non-woven fabric (S) and
melt blown non-woven fabric (M/S.times.100(%)) may be in the range
of 20% to 200%. In case of less than 50%, the gaps between the
fibers become larger thereby hard to maintain the water resistance.
In case of more than 200%, tension strength of the non-woven fabric
decreases thereby getting brittle. In addition, the water pressure
resistance of the hydrophobic non-woven fabric layer is in the
range of more than 100 mmH.sub.2O or more, and preferably in the
range of 150 mmH.sub.2O or more.
[0172] In case of using these non-woven fabric made from the spun
bond non-woven fabric (S) and melt blown non-woven fabric (M) as
the non-woven fabric constituting the hydrophobic non-woven fabric
layer, the apparent fineness of the filament constituting the layer
of the spun bond non-woven fabric is preferably in the range of 3.0
denier or less. In case of more than 3.0 denier, it becomes rough
and gets feeling bad.
[0173] The weight of the non-woven fabric is preferably in the
range of 10 to 50 g/m.sup.2. In case of less than 10 g/m.sup.2, the
strength becomes lower, and in case of more than 50 g/m.sup.2, the
stiffness becomes larger, and the costs increase. Both cases are
adverse.
[0174] (The Fine Cellulose Fiber Layer)
[0175] In the highly air-permeable and water-resistance sheet
according to the present invention, the fine cellulose fiber layer
is a layer comprising a cellulose in the form of micro fine fiber
(hereinafter, also referred to as "fine cellulose fiber") wherein
the cellulose fiber of cellulose or cellulose derivative is
mechanically and/or chemically treated to form the fine cellulose
fiber.
[0176] The fine cellulose fiber in the present invention includes a
material that a slurry of pulp made from the cellulose or cellulose
derivative is mechanically fibrillated. In addition, it includes
bacterial cellulose made from bacterium such as acetobacter. In
particular, it includes hydrous microfibrillated cellulose fiber
(MFC; Micro Fibrillated Cellulose). Here, the hydrous
microfibrillated cellulose fiber will be explained in more
detail.
[0177] MFC is an abbreviation of Micro Fibrillated Cellulose and is
called as fine fibrillated cellulose in the art. Among them, it is
called biocellulose (BC) which is originated from microorganism.
These celluloses are disclosed in, for example, Patent-related
Document 3 and the biocellulose is disclosed in Non-Patent-related
Document 1.
[0178] The weight of the non-woven fabric used in the present
invention is preferably in the range of 10 to 50 g/m.sup.2, more
preferably in the range of 12.0 to 20 g/m.sup.2. In case of less
than 10 g/m.sup.2 of the weight, it is not preferable, since the
strength is shortened, and the water resistance becomes lower
thereby easily leakage of urine when it is used in the absorbent
article. In addition, In case of more than 50 g/m.sup.2 of the
weight, it is not preferable, since the thickness of the sheet
becomes thin and the stiffness is high and the cost thereof is
high. In addition, the weight of the fine cellulose fiber layer is
preferably in the range of 2.0 to 20.0 g/m.sup.2, more preferably
in the range of 4.0 to 10.0 g/m.sup.2. In case of less than 2.0
g/m.sup.2 of the weight, it is not preferable, since the water
resistance becomes lower thereby easily leakage of urine when it is
used in the absorbent article. On the other hand, in case of more
than 20.0 g/m.sup.2 of the weight, it is not preferable, since the
fine cellulose fiber layer and the hydrophobic non-woven fabric
layer cannot be integrated, the delamination becomes occur, and the
costs thereof becomes high.
[0179] In the highly air-permeable and water-resistance sheet
according to the present invention, the average length of the fine
cellulose fiber constituting the fine cellulose fiber layer is
preferably 0.3 mm or less. In case of more than 0.3 mm, the fibers
are easily entangled each other, the sheet formability becomes less
and the penetration into the hydrophobic non-woven fabric layer
becomes difficult. Further, the hydration capacity of the fine
cellulose fiber is preferably in the range of 15 mL/g or more. In
case of less than 15 mL/g, it is hard to obtain a slurry having
stable dispersibility.
[0180] It should be noted that the above-mentioned hydration
capacity may be measured in the following method. That is, the fine
cellulose fiber (0.5 g) is weighed in the centrifugiable test tube
(30 mm.times.100 mm, volume 50 mL) and introduced into water to
obtain 50 mL of a water dispersion liquid. Then, it is centrifuged
at 2000.times.g (3300 rpm) for 10 minutes and examine the volume of
the precipitate. The obtained values are substituted in the
following equation to obtain the hydration capacity.
Hydration capacity (mL/g)=Volume of the precipitate (mL)/weight of
the fine cellulose fiber (g)
[0181] (The Water Repellant Layer)
[0182] The highly air-permeable and water-resistance sheet
according to the present invention comprises the water repellant
layer on either or both of the surfaces of the composite sheet
comprising the above-mentioned hydrophobic non-woven fabric layer
and the fine cellulose fiber layer. Thereby, the highly
air-permeable and water-resistance sheet according to the present
invention can provide an effect originated from the component
constituting the water repellant layer. Materials as used in the
water repellant layer include several materials having water
repellency such as silicones, Teflon (Trade mark), paraffin waxes
as well-known in the art. Among them, the preferred water repellant
includes an emulsion which is emulsified and dispersed in the form
of oil in water (O/W). Thereby, it is possible to be appropriately
subject to water repellant treatment to the water repellant layer
even in the case that the component of the composite sheet
consisted of the hydrophobic non-woven fabric layer and the fine
cellulose fiber layer has different physical interaction due to the
difference of the melting concentration and the type. In
particular, in view of the cost and air permeability after the
water repellant treatment, olefinic water repellent is preferable.
The olefinic water repellent includes a matter mainly containing
natural wax, synthetic wax and fatty acid derivatives. The type of
the olefinic water repellent is not limited, but includes in the
form of emulsion. The solid concentration of these olefinic water
repellents is preferably in the range of 30 to 50 weight %. In case
of less than 30 weight %, it is easily flowed to become unevenness.
In case of more that 50 weight % it becomes viscosity to hard to
handle it.
[0183] In the highly air-permeable and water-resistance sheet
according to the present invention, the water repellant layer may
contain resins in addition to the above-mentioned water repellant
to improve water resistance. The resins include stylene resins,
acrylate resins, polyester resins, ethylene resins, urea resins,
melamine resins, ethylene-urea resins, glyoxal resins, or copolymer
thereof. Among them, the synthetic resin binder is preferable,
including stylene-butadiene resins, acrylate resins, polyester
resins, ethylene-vinyl acetate copolymer. In particular,
stylene-butadiene resin (SBR) is more preferable as the resins, in
view of improvement of the water resistance due to formation of
film state, and compatibility to the olefinic water repellent.
[0184] In addition, in the highly air-permeable and
water-resistance sheet according to the present invention, in
addition to the above-mentioned materials, the water repellant
layer may contain the cross linker in order to stably provide the
effect originated from the components of the water repellant layer.
The cross linker includes polyamide epichlorohydrin resins,
polyamine epichlorohydrin resins, melamine resins, urea resins,
ketone resins, glyoxal, ammonia zirconium carbonate. In particular,
ammonia zirconium carbonate is preferable, since it is to provide
sustained effect of the water resistance and water repellent by
means of directly crosslinking carboxyl group and hydroxy group of
ammonia zirconium carbonate with the above-mentioned resins and
water repellent.
[0185] In the highly air-permeable and water-resistance sheet
according to the present invention, the relative ratio of the
olefinic water repellent and the synthetic resin binder is
preferably in the range of 40/60 to 70/30, more preferably in the
range of 45/55 to 60/40. In addition, the content of the cross
linker added as the components of the water repellant layer
(especially, zirconium cross linker) is in the range of 2 to 4
parts relative to 100 parts of total content of the olefinic water
repellent and the synthetic resin binder. In case of more than 4
parts, pot life of the coating composition is shortened, and in
case of less than 2 parts, enough effect of the water resistance
and water repellency cannot be obtained.
[0186] The water repellant treatment method to the composite of the
hydrophobic non-woven fabric layer/fine cellulose fiber layer
(composite sheet) with water repellant layer may use in accordance
with the general coating method. For example, it includes air knife
method, mayerbar coating method, gravure method, offset gravure
method, micro gravure method, flexographic method, reverse roll
method, blade method, curtain method, dye method. The amount of the
coating is preferably in the range of 1.0 to 10.0 g/m.sup.2, more
preferably in the range of 1.5 to 3.0 g/m.sup.2. In case of less
than 1.0 g/m.sup.2, enough property of water resistance and water
repellency cannot be obtained, in case of more than 10.0 g/m.sup.2,
the water resistance property becomes almost saturated state, and
the cost becomes high.
[0187] Further, in the highly air-permeable and water-resistance
sheet according to the present invention, the water repellant layer
may contain a deodorizer in addition to the above-mentioned
components. Several materials as well-known in the art can be used
as the deodorizer so far as the deodorizer can adsorb the gas
molecule such as volatile composition. For example, it includes
zeolite originated from natural resources, synthetic zeolite,
synthetic clay, sepiolite, white clay, activated carbon,
CaCO.sub.3, titanium dioxide, cupper carboxymethyl cellulose
(Cupper CMC), trivalent ferric ion, silver compounds (zeolite
supporting silver), metal oxides, catechin. Among them, the zeolite
originated from natural resources is most preferable in overall
consideration of deodorization performance, cost and
appearance.
[0188] The content of the deodorizer contained in the water
repellant layer may be appropriately selected in accordance with
type of deodorizer and desired effect. For example, the content of
the deodorizer in the water repellant layer is preferably in the
range of 0.5 to 10.0 g/m.sup.2, more preferably in the range of
1.5-6.0 g/m.sup.2. In case of less than 0.5 g/m.sup.2, enough
deodorization performance may not be sometimes obtained, and in
case of more than 10.0 g/m.sup.2, the deodorization performance is
almost saturated, and it is disadvantage in view of the cost.
[0189] <The Highly Air-Permeable and Water-Resistance Sheet
Composite According to the Present Invention>
[0190] As shown in FIGS. 2a and 2b, a highly air-permeable and
water-resistance sheet composite 20 according to the present
invention has a structure that a non-woven fabric layer 15 is
layered on the water repellant layer of the above-mentioned highly
air-permeable and water-resistance sheet according to the present
invention. That is, the highly air-permeable and water-resistance
sheet composite according to the present invention is characterized
in that it comprises the hydrophobic non-woven fabric layer 14, the
fine cellulose fiber layer 12 layered on the hydrophobic non-woven
fabric layer 14, the water repellant layer 13 layered on the fine
cellulose fiber layer, and the non-woven fabric layer 15 layered
onto the water repellant layer 13. The highly air-permeable and
water-resistance sheet composite according to the present invention
may comprise the fine cellulose fiber layer 12 between the water
repellant layer 13 and the non-woven fabric layer 15 as shown in
FIG. 2b. In addition, the highly air-permeable and water-resistance
sheet composite according to the present invention may comprise the
water repellant layer 13 further layered on the non-woven fabric
layer 15, not shown in the Drawing. It should be noted that the
non-woven fabric layer 15 may be the same as the hydrophobic
non-woven fabric layer 14.
[0191] In highly air-permeable and water-resistance sheet composite
according to the present invention, the fine cellulose fiber layer
12, the water repellant layer 13 and the hydrophobic non-woven
fabric layer 14 may used as the same as those of the highly
air-permeable and water-resistance sheet according to the present
invention as mentioned above. In particular, the non-woven fabric
layer 15 layered onto the water repellant layer 13 may be the
above-mentioned hydrophobic non-woven fabric layer. However, in
case that a water resistance is not so much desired, it is
convenient to use several types of non-woven fabrics.
[0192] The highly air-permeable and water-resistance sheet
composite according to the present invention comprises the
non-woven fabric layer 15 onto the water repellant layer 13.
Accordingly, the water repellant layer 13 covering the fine
cellulose fiber constituting the fine cellulose fiber layer layered
on the hydrophobic non-woven fabric layer 14 will be physically
isolated from the surface of the highly air-permeable and
water-resistance sheet composite. Therefore, the fine cellulose
fiber layer covered with the component constituting the water
repellant layer will be protected from the physical forces such as
ablation, thereby improving the durability. In addition, the highly
air-permeable and water-resistance sheet composite according to the
present invention is the combination of the hydrophobic non-woven
fabric layer, the fine cellulose fiber layer and the water
repellant layer. Accordingly, it is possible to prevent the passage
of microorganism and fine particles. Further, the highly
air-permeable and water-resistance sheet composite according to the
present invention is constituted such that it maintains its air
permeability. Accordingly, the provision of the function from the
functional component contained in the water repellant layer and the
others such as the deodorizer is not affected, although it has a
multilayered structure. Therefore, the highly air-permeable and
water-resistance sheet composite according to the present invention
is practically useful.
[0193] <Method for Manufacturing the Highly Air-Permeable and
Water-Resistance Sheet According to the Present Invention>
[0194] Next, the method for manufacturing the highly air-permeable
and water-resistance sheet according to the present invention will
be explained. The method for manufacturing a highly air-permeable
and water-resistance sheet according to the present invention
comprises the steps of degassing the hydrophobic non-woven fabric
layer using a degassing medium containing water, of layering a fine
cellulose fiber layer on so degassed hydrophobic non-woven fabric
layer, and of layering a water repellant layer on said fine
cellulose fiber layer. Hereinafter, each of steps is also referred
to as a degassing step, a fine cellulose fiber layer layering step
and a water repellant layer layering step. Here, each step will be
explained in below.
[0195] (The Degassing Step)
[0196] In the method for manufacturing a highly air-permeable and
water-resistance sheet according to the present invention, the
hydrophobic non-woven fabric layer consisting of the non-woven
fabric is preliminarily degassed using the degassing medium
containing water in order to uniformly layer the fine cellulose
fiber layer. By this degassing step, gasses such as air contained
in the hydrophobic non-woven fabric layer will be removed from the
hydrophobic non-woven fabric layer and replaced with the degassing
medium. The so degassed hydrophobic non-woven fabric layer will be
filled up and saturated with the degassing medium. Therefore, in
the present invention, the degassing medium is also referred to as
a saturation medium. It should be noted that the degassing step is
repeated with several times using same or different degassing
medium.
[0197] Water, especially deionized water is generally used as the
degassing medium. However, the degassing medium is not limited so
far as it contains water. The degassing medium may contain a
hydrophilic organic solvent and a surface-activating agent in order
to enhance the uniform coating of the slurry such as MFC slurry
used for layering fine cellulose fiber layer to the hydrophobic
non-woven fabric layer when the fine cellulose fiber layer is
layered as the following step.
[0198] The hydrophilic organic solvent contained in the degassing
medium in addition to water includes alcohols such as methanol,
ethanol and propanol. In particular, the hydrophilic organic
solvent is preferably ethanol. The content of the hydrophilic
organic solvent is desirably in the range of 50% or more relative
to the volume of the degassing medium in view of the cost and
handling thereof.
[0199] In case of using water only as the degassing medium, it is
necessary to contain small amount of the surface-activating agent
in water in order to well maintain the wettability of the surface
of the hydrophobic non-woven fabric layer. Cationic, anionic or
nonionic agent of the mixture thereof can be used as the
surface-activating agent. Representatives include nonionic agent or
anionic agent which has good permeability, or mixture thereof.
Nonionic agent includes an adduct of nonylphenol ethylene oxide
such as polyoxyethylene (10) nonylphenylether (NPEO). Anionic agent
includes for example dodecylbenzene sulfonic acid (LAS). Mixture of
NPEO and LAS is one of the preferable surface-activating agents.
Although the detergents as commercially available may be used,
single component of the agent is preferably used in consideration
of the recovering or drainage treatment.
[0200] The content of the surface-activating agent in the degassing
medium is determined in accordance with CMC (Critical Micelle
Concentration), and is preferably in the range of 100 to 1000 ppm.
If the surface-activating agent is remained in the sheet, the water
resistant property is affected. So, the content is preferably lower
as possible. For this purpose, for example, the following method is
selected. That is, the hydrophobic non-woven fabric layer is
subjected to the surface treatment with a small amount liquid
containing the relative high concentration of the
surface-activating agent to preliminarily adsorb the
surface-activating agent on the surface of the hydrophobic
non-woven fabric layer. After that, the sheet is saturated with
large amount of water. For example, in case of using NPEO, 300 to
500 ppm of the activated agent in aqueous solution is sprayed on
the hydrophobic non-woven fabric layer at 100% of the weight
thereof (if the weight of the non-woven fabric is 15 g/m.sup.2, the
sprayed solution is 15 g/m.sup.2). After that, the hydrophobic
non-woven fabric layer is sufficiently filled up and saturated with
20 times of the deionized water.
[0201] (The Fine Cellulose Fiber Layer Layering Step)
[0202] In the method for manufacturing a highly air-permeable and
water-resistance sheet according to the present invention, the
composite sheet comprising the hydrophobic non-woven fabric layer
and the fine cellulose fiber layer layered on the hydrophobic
non-woven fabric layer is manufactured by layering the hydrophobic
non-woven fabric layer and the fine cellulose fiber layer in the
fine cellulose fiber layer layering step in accordance with several
layering technique. For example, the technique includes the wet
forming method in which the following dispersion liquid containing
the component constituent the fine cellulose fiber layer is spread
on the hydrophobic non-woven fabric layer using papermaking machine
and others to form a layered product of hydrophobic non-woven
fabric layer/fine cellulose fiber layer, and a method in which high
viscous slurry is coated on the carrier sheet to form a thin layer
of fine cellulose fiber, the thin layer is delaminated from the
carrier sheet, and is bonded to the hydrophobic non-woven fabric to
form the layered product of hydrophobic non-woven fabric
layer/hydrophobic non-woven fabric layer.
[0203] In particular, in the present invention, in case of layering
the fine cellulose fiber layer on the hydrophobic non-woven fabric
layer, the following coating method using slurry of the fine
cellulose fiber containing water is to have an advantage, in
consideration of the hydrophobicity of the hydrophobic non-woven
fabric layer and the hydrophilicity of the fine cellulose fiber
layer.
[0204] That is:
[0205] (1) means for directly coating with a water dispersion
slurry in which, after the substrate is treated to be hydrophilic
with the surface-activating agent, the water dispersion slurry
containing the component of the fine cellulose fiber layer such as
MFC is directly coated to the obtained substrate;
[0206] (2) means for directly coating the substrate with a water
dispersion slurry in which the surface-activating agent is added to
the above-mentioned slurry, and a penetration ability is provided;
and
[0207] (3) means for directly coating the substrate with a
dispersion slurry using a mixed solvent of water and an organic
solvent as a dispersion medium for preparing a dispersion slurry
containing the component of the fine cellulose fiber layer, wherein
the organic solvent has a penetration ability to the substrate and
can stably disperse the fine cellulose fiber such as MFC.
[0208] In particular, the above-mentioned means (1) is a preferable
method in view of enhancing the uniformity. In addition, the
above-mentioned means (3) is a preferable method in view of
enhancing the water pressure resistance.
[0209] In case of directly coating method, the high viscous slurry
of MFC dispersion liquid is directly coated on the hydrophobic
non-woven fabric layer, and then the liquid is removed, and dried.
Thereby, the layered product comprising extremely thin layer of the
fine cellulose fiber layer having 0.5 to 5 g/m.sup.2 which cannot
be achieved in the prior art. The fine cellulose fiber layer has
dense structure like parchment paper, and also has s porous
structure having a plurality of pores. In the dry state, since the
normal microorganisms cannot be passed thorough the pore, it can be
applied as a layer having a barrier against bacteria.
[0210] In addition, in consideration of the binding state of the
hydrophobic non-woven fabric layer and the fine cellulose fiber
layer, the obtained product after the above-mentioned layering may
be subjected to heat press treatment. In addition, binding agent
such as E.V.A. emulsion is added to the dispersion liquid, and
after the desolvation of the slurry is performed, it may be
subjected to heat treatment. By these treatments, it is possible to
obtain the composite sheet in stable combined state.
[0211] The water mixable solvent in the preparation of the
dispersion liquid containing the component constituting the fine
cellulose fiber layer is not limited so far as it has compatible to
water. Example of such a solvent includes methyl alcohol, ethyl
alcohol, isopropyl alcohol, ethylene glycol, propylene glycol,
dioxane, aetone, tetrahydro furan, glycerine, neopentylglycol,
pentaerythritol and dimethyl sulfoxide. In particular, ethyl
alcohol is preferably used as the solvent.
[0212] The dispersion liquid (hereinafter, also referred to as
"slurry") used for layering the fine cellulose fiber layer may be
manufactured in which the component constituting the fine cellulose
fiber layer such as MFC is added to the above-mentioned liquid
medium or to a mixed medium of water and the solvent, and it is
applied with an appropriate shear force/agitation force to prepare
the uniform dispersion liquid.
[0213] In case of using, for example, MFC as the component of the
fine cellulose fiber layer in the preparation of the dispersion
liquid, a stable dispersion liquid of MFC and the following
additive particle (if it is) is formed due to the viscosity of the
MFC in the liquid medium. It should be noted that it is preferable
to use the method based on Patent-related Document 4 as proposed by
the present inventors in order to efficiently manufacturing the
water dispersion liquid used in the present invention.
[0214] The MFC concentration in the MFC slurry is preferable in the
range of 3% or less, since the slurry has high viscosity. It is
more preferable that the concentration is in the range of 0.5 to
2.0 weight % in view of the coating performance.
[0215] MFC is obtained as partly swelled MFC paste in the hydrated
state by continuously beating and grinding under high pressure the
wood pulp solution having 2 to 5 weight % of dispersion
concentration in the water medium for long time. In case of BC, BC
paste in the hydrated state having 0.1 to 2.0 weight % of the
concentration is obtained by which the fine cellulose fiber is
created from the acetobacter by culturing the acetobacter in the
aqueous solution medium, and the created fine cellulose fiber is
purified, aggregated and concentrated.
[0216] The MFC and BC pastes is difficult to handle as fluid, since
these have extremely high viscosity themselves. Accordingly, it is
preferable to prepare it as dispersion liquid which is easily
handled by diluting it to 2 weight % or lower of the concentration.
Water and an organic solvent such as ethanol are generally used as
the diluent. It should be noted that polyvalent alcohol such as
polyethylene glycol, propylene glycol and glycerin may be added in
the diluent as plasticizer in order to prevent the creation of the
shrinked ruck and/or cruck along with overdry of MFC in following
drying process.
[0217] (The Water Repellant Layer Layering Step)
[0218] In the method for manufacturing the highly air-permeable and
water-resistance sheet according to the present invention, a method
for carrying out the water repellant layer layering step is not
limited so far as the water repellant layer is layered on either or
both of surfaces of the composite sheet comprising the hydrophobic
non-woven fabric layer and the fine cellulose fiber layer which are
layered as mentioned above. The water repellant treatment includes
the well-known method such as spray coating with spraying the water
repellant, roll coater and brush coater.
[0219] In the method for manufacturing the highly air-permeable and
water-resistance sheet according to the present invention, the
water repellant treatment may be subjected to one side or both
sides of the layered product of the hydrophobic non-woven fabric
layer/fine cellulose fiber layer. In case of treating one side of
the layered product of the hydrophobic non-woven fabric layer/fine
cellulose fiber layer, it is preferably treated on the side of the
fine cellulose fiber layer. Thereby, the hydrophilicity and the
water penetrating property of the cellulose is blocked, and the
stable water proof and water repellency can be maintained with the
combined effect of the hydrophobic non-woven fabric layer.
[0220] FIGS. 3A to 3E show the schematic view of example of these
methods for manufacturing the highly air-permeable and
water-resistance sheet according to the present invention. These
figures are a flowchart showing a method for manufacturing the
highly air-permeable and water-resistance sheet according to the
present invention. As referred to FIGS. 3A to 3E, the substrate
constituting the hydrophobic non-woven fabric layer is supplied
from roller in the wound form into the system by an action such as
an unreel (substrate unreel). The substrate is filled up and
saturated with the degassing medium such as water and solvent
constituting the above-mentioned dispersion liquid in order to
degas the air contained in the substrate (pretreatment of the
substrate). After that, the dispersion liquid such as MFC slurry
which is previously prepared is coated on the substrate, as shown
in FIGS. 3A to 3E. After the solid component constituting the
dispersion liquid is brought into a predetermined shape on the
substrate, the medium of the dispersion liquid is removed using
vacuum pump (vacuum suction treatment).
[0221] The vacuum treated composite sheet (the layered product of
hydrophobic non-woven fabric layer/fine cellulose fiber layer) may
be then dried and fixed (see FIG. 3A). In addition, the vacuum
treated layered product of hydrophobic non-woven fabric layer/fine
cellulose fiber layer may be re-coated with the dispersion liquid
(after coat; see FIG. 3C). In addition, the vacuum treated layered
product of hydrophobic non-woven fabric layer/fine cellulose fiber
layer may be water squeezed by the press apparatus thorough the
felt (squeezing by the press; see FIGS. 3D and 3E). As not shown in
Figures, the layered product of the hydrophobic non-woven fabric
layer/fine cellulose fiber layer may be dried and fixed.
[0222] On the other hand, the layered product of the hydrophobic
non-woven fabric layer/fine cellulose fiber layer which is vacuum
treated or dried and fixed is subjected to the water repellant
treatment (Water repellant treatment; FIGS. 3A to 3E). The method
for preparing the water repellant layer is not limited so far as
the above-mentioned water repellant such as the olefinic water
repellent, resins such as the synthetic resin binder, and the cross
linker such as ammonia zirconium carbonate are uniformly mixed at
the predetermine ratio and the timing of mixing. For example, after
a main agent comprising the water repellant such as the olefinic
water repellent and resins such as the synthetic resin binder are
prepared by mixing at the predetermined ratio under stirring, the
cross linker may be added at the last minute of the coating to the
composite sheet under stirring along with the addition of water to
prepare the coating composition having the predetermined
concentration and viscosity.
[0223] After the water repellant treatment, the layered product of
the hydrophobic non-woven fabric layer/fine cellulose fiber layer
may be heat treated and fixed. At this heat treatment and fixation,
it may be simultaneously dried. In addition, the heated layered
product of the hydrophobic non-woven fabric layer/fine cellulose
fiber layer may be subjected to the calendaring treatment (see
calendaring treatment; FIGS. 3D and 3E). In addition, in the
present invention, it may be further heat treated in order to
improve the water resistance after the calendaring treatment. The
fine cellulose fiber layer constituting the composite sheet has
high resistance to high temperature and hard to be easily fused. On
the other hand, the hydrophobic non-woven fabric layer is
relatively thermally fused. When the thermal treatment equipment is
combined with the heat roller and cooling roller, the side of the
fine cellulose fiber layer is in contact with the heat roller, the
side of the hydrophobic non-woven fabric layer is in contact with
the cooling roller and the heat press treatment is performed, the
surface of the hydrophobic non-woven fabric layer is partially
fused, the fused part is penetrated and adhered to the fine
cellulose fiber layer, the integration of the fine cellulose fiber
layer with the hydrophobic non-woven fabric layer, the thickness
thereof becomes lower and the water resistance can be improved. In
case of, as hydrophobic non-woven fabric layer, the using spun melt
non-woven fabric of sheath/core type composite fiber such like as
PE/PET spun bond and PE/PP spun bond comprising an easily fusible
component as sheath and relatively-hard-to-fuse component as core,
it is possible to easily and conveniently perform the heat
treatment. It should be noted that although the manufacturing step
of the composite sheet and the layering step of the water repellant
layer are shown as continuous steps in FIGS. 3A to 3E, the highly
air-permeable and water-resistance sheet may be manufactured by the
steps as separated each other.
[0224] <Apparatus for Manufacturing the Highly Air-Permeable and
Water-Resistance Sheet According to the Present Invention>
[0225] Next, an example of the apparatus for manufacturing the
highly air-permeable and water-resistance sheet according to the
present invention will be explained with reference to FIGS. 4A to
6.
[0226] FIG. 4A is a schematic view of the coating unit in the
apparatus for manufacturing the highly air-permeable and
water-resistance sheet according to the present invention. A sheet
(substrate) 200 constituting the hydrophobic non-woven fabric layer
unreeled from an unreeler 232 is positioned on a net conveyer 210
carried with a roller 222. A coating slurry 202 and a saturation
medium 204 are supplied on the surface of the sheet 200 from a head
box 212 and a saturation medium supplier 214 in synchronization
with the movement of the sheet 200. After that, the sheet 200 is
moved and passed through between the coating roller 220 and the net
conveyer 210, and removed liquid with a vacuum unit 234 connected
with the vacuum pump (not shown in Figures) and progressed in the
further steps.
[0227] A unreel apparatus for manufacturing paper and the normal
non-woven fabric may be sued as the unreeler 232. Although the
unreeled substrate may be carried in the coating unit by the
roller, the substrate is generally carried on the net conveyer 210
as supporting body as shown in FIG. 4A.
[0228] Next, the pretreatment of the substrate and the slurry
coating to the substrate will be explained in detail with reference
to FIGS. 4B, 5A to 5C, and 6.
[0229] FIG. 4B is an enlarged view of FIG. 4A, indicating the
proximity of the coating roller 220. The saturation medium 204 is
supplied from the saturation medium supplier 214 on the moving
sheet 200. After that, the coating slurry 202 supplied from the
head box 212 is supplied on the sheet 200, and the coating slurry
202 is positioned by the rotation of the coating roller 220 on the
sheet 200 in synchronization with the movement of the sheet 200
moving on the net conveyer 210.
[0230] The saturation medium 204 may be supplied on the upstream
position at which the coating slurry 202 is supplied as shown in
FIGS. 4B and 5A. The saturation medium 204 may be supplied in
accordance with the method for spreading state as shown in FIG. 4B,
or may be supplied on the sheet in the droplet form as shown in
FIG. 5A. A water stream 244 which is supplied and formed as
mentioned above is only left for the removal of extra water at the
narrow portion of coater header in accordance with the movement of
the net conveyer 210 and water stream is transferred through the
hydrophobic non-woven fabric layer to the conveyer. Thereby, the
medium in the sheet will block the air collectively flow into the
mechanical gap during the coating operation, it is mixed finally
with the coating slurry to penetrate into the substrate, thereby
forming the fine cellulose fiber layer (coating layer) on the
sheet. On the other hand, the saturation medium may be supplied on
the sheet in the shower form as shown in FIG. 6. It should be noted
that the saturation medium 204 is not limited so far as it is
filled up with the void of the sheet 200 and the sheet is degassed
with such a liquid (degassing medium). For example, such a liquid
is preferably water, or mixed solvent of water and an organic
solvent, constituting the above-mentioned dispersion liquid.
[0231] <The Method for Manufacturing a Highly Air-Permeable and
Water-Resistance Sheet Composite According to the Present Invention
and an Apparatus for Manufacturing Thereof>
[0232] The method for manufacturing a highly air-permeable and
water-resistance sheet composite according to the present invention
comprises the degassing step, the fine cellulose fiber layer
layering step and the water repellant layer layering step as
mentioned in the method for manufacturing a highly air-permeable
and water-resistance sheet, and further comprises a step of further
layering a layer having a non-woven fabric onto the water repellant
layer. Hereinafter, the step is also referred to as a non-woven
fabric layering step, and explained.
[0233] In the method for manufacturing a highly air-permeable and
water-resistance sheet composite according to the present
invention, the non-woven fabric layering step is not limited so far
as it is a method for layering the above-mentioned non-woven fabric
layer on to the water repellant layer.
[0234] In the non-woven fabric layering step, what is layered onto
the water repellant layer may be the non-woven fabric layer. In the
non-woven fabric layering step, in case of using the non-woven
fabric layer, the highly air-permeable and water-resistance sheet
composite as shown in FIG. 2a will be obtained.
[0235] In addition, in the non-woven fabric layering step, what is
layered onto the water repellant layer may be as the composite
sheet comprising the non-woven fabric layer and the fine cellulose
fiber layer layered on the non-woven fabric layer. The non-woven
fabric layering step is performed such that, in case of using the
composite sheet, the fine cellulose fiber layer of the composite
sheet is in contact with the water repellant layer. Thereby, the
highly air-permeable and water-resistance sheet composite as shown
in FIG. 2b will be obtained.
[0236] In addition, the method for manufacturing a highly
air-permeable and water-resistance sheet composite according to the
present invention may further comprises a step of further layering
the fine cellulose fiber layer on the water repellant layer between
the water repellant layer layering step and the non-woven fabric
layering step wherein the a step of further layering the fine
cellulose fiber layer is also referred to as a fine cellulose fiber
layer layering second step. The fine cellulose fiber layer layering
second step may be performed as the same method mentioned in the
fine cellulose fiber layer layering step.
[0237] It should be noted that the non-woven fabric layer used in
these non-woven fabric layering step and fine cellulose fiber layer
layering second step may be of degassing it using the degassing
medium in accordance with the above-mentioned degassing step.
[0238] <The Absorbent Article According to the Present
Invention>
[0239] Next, the absorbent article according to the present
invention will be explained with reference to Figures. FIG. 7 is a
partial schematic cross section view of the absorbent article
according to one aspect of the present invention, and FIG. 8 is a
partial schematic cross section view of the absorbent article
according to another aspect of the present invention. Both of the
absorbent article comprises an absorbent body 16 on either surface
of the above-mentioned highly air-permeable and water-resistance
sheet. In addition, absorbent article according to the present
invention may comprise the absorbent body 16 on either surface of
the above-mentioned highly air-permeable and water-resistance sheet
composite.
[0240] (The Absorbent Body)
[0241] In the absorbent article according to the present invention,
materials, aspect, constitution and the other of the absorbent body
16 is not limited so far as it can absorb any fluids such as body
fluid. The absorbent body includes highly water absorptive polymer
such as SAP (superabsorbent polymer) in the powder form, wood pulp
having fluid retention, fluff pulp milled the wood pulp and mixture
thereof. In particular, it is preferable an aspect that
thermoplastic resin, fluff pulp and highly water absorptive polymer
are mixed and the mixture is processed into the matted form. The
highly water absorptive polymer may be used as mixture with fluff
pulp, and may be added to the fluff pulp to be partially
incorporated into the pulp. It is preferable the highly water
absorptive polymer which has a retention property that 20 times or
more of liquid relative to its weight can be absorbed and retained,
and which is in the particle form having a property capable of
forming gel. Such a highly water absorptive polymer includes
starches, celluloses and synthetic polymers. In particular, it
preferably includes starch-acrylate graft copolymer, saponified
product of starch-acrylonitrile copolymer, cross-linked product of
sodium carboxymethyl cellulose, and acrylate polymer. Among them,
in consideration of morphological stability, and possible drop off,
it is preferable the absorbent body in the sheet form in which SAP
is processed into the sheet form. An absorbent body in the sheet
form comprising SAP as a main component will be explained.
[0242] FIG. 10 is views showing one aspects of absorbent body in
the sheet form used for the absorbent article according to the
present invention, wherein (a), (c) and (d) indicate plan views
thereof and (b) indicates the cross-sectional view of (a). In FIG.
10, "phase A" indicates a region having water absorbent materials
such as SAP, "phase B" indicates a region not having the water
absorbent material. In the absorbent article according to the
present invention, the absorbent body may comprise the phase A
which is positioned to extend to the longitudinal direction of the
absorbent body, and the phase B which is positioned in the parallel
direction of the phase A, as shown in FIGS. 10 (a) and (b). The
phase A plays a function which absorbs the liquid such as body
fluid. In addition, the phase B plays a function of penetration,
dispersion and acquisition of the liquid. In case of such as aspect
of the absorbent body, the excreted body fluid is dispersed and
penetrated though the phase B, and is in contact with and
sequentially absorbed in SAP of the phase A which has a wide area,
thereby retaining in the phase A.
[0243] In the present invention, the absorbent body in the sheet
form is not limited to the aspect as exemplified in FIGS. 10 (a)
and (b), and may include an aspect that the phase A is
discontinuously arranged in the phase B which is continuously
arranged as shown in FIG. 10 (c). In addition, the absorbent body
may include an aspect that the phase B is discontinuously arranged
in the phase A which is continuously arranged, as shown in FIG. 10
(d). The aspect of the phase A and/or phase B which are
discontinuously arranged may include any shapes such as
rectangular, circular and triangular shapes.
[0244] Generally, the air permeability of the absorbent article is
greatly affected to the air permeability of the backsheet prior to
absorbing the body fluid, and is also greatly affected to the
structure of the absorbent body after absorbing the body fluid.
This is based on that the absorbent body is swelled to block the
passage of air. Therefore, in the present invention, the following
constitution will be selected in order to adjust the air
permeability of the absorbent body before and after absorbing the
body fluid. Thereby, the absorbent article according to the present
invention can secure enough air permeability even after it has
absorbed the body fluid.
[0245] The absorbent body in the sheet form is preferably that the
highly water absorptive sheet has 50 weight % or more of SAP,
preferably 60 to 95 weight % of SAP. In addition, the thickness of
the absorbent body is preferably in the range of 1.5 mm or lower,
more preferably in the range of 1 mm or lower. In case of less than
50 weight %, the thickness of the absorbent body hard to
decrease.
[0246] Structure of the absorbent body used in the absorbent
article according to the present invention, and a method for
manufacturing the absorbent body are not limited. The method for
manufacturing the absorbent body includes the Air Laid method; the
Coating method using a slurry comprising components for the
absorbent body; a method for immobilizing SAP in which a large
amount of SAP is supported in a raised non-woven fabric, and SAP is
immobilized with hotmelt binder, emulsion binder or aqueous fiber
and the others; a method for forming a fibrous SAP into the web
form by mixing with PET (polyethylene terephthalate) fiber; and a
method for forming in which both surfaces of SAP layer are
sandwiched with a tissue.
[0247] (Other Members)
[0248] In the absorbent article according to the present invention,
several types of members such as so-called buffer sheet are
provided in accordance with use of the absorbent article. The use
of the absorbent article includes, for example, a case that the
body fluid is efficiently processed even though a large amount of
the body fluid is loaded to the absorbent article under pressure.
As such a case, when the infant is used after he sleeps all night,
and when the diaper for adult is used in the bedridden state or sat
state, the body fluid is sometimes adequately absorbed and a load
is locally applied for a long time in the absorbent body in the
saturated state. When the highly air-permeable and water-resistance
sheet according to the present invention is used in such a case,
the body fluid is gradually permeated into the highly air-permeable
and water-resistance sheet and the body fluid will be sometimes
leaked. In order to deal with such a situation, means for prevent
the effect of the load is effective by means of partially
positioning non-porous PE film and air permeable film at the loaded
portion. However, the combination of such films will lead to loss
of air permeability of the absorbent article even in the case of
combining the air permeable film. Accordingly, it is necessary to
confine the application of non-porous PE film to 1/3 area of the
whole area of the highly air-permeable and water-resistance sheet.
As an effective means which will not affect the air permeability
and prevent such a leakage, it is preferable that porous buffer
sheet is provided between the absorbent body and the highly
air-permeable and water-resistance sheet according to the present
invention. Thereby, it is possible to disperse the weight load and
prevent the leakage even though the load is applied as mentioned
above. As an example of such a buffer sheet, FIG. 9 is a partial
schematic cross section view of the absorbent article according to
the present invention further comprising an apertured film. In the
Figure, an absorbent article 100 further comprises an apertured
film 18 between the highly air-permeable and water-resistance sheet
constituting the above-mentioned absorbent article and the
absorbent body. Although the Figure shows that the apertured film
18 is provided between the hydrophobic non-woven fabric layer 14
and the absorbent body 16 of the highly air-permeable and
water-resistance sheet, the apertured film 18 may be provided on
the fine cellulose fiber layer 12, and there may be absorbent body
16 on the apertured film 18, by inverting the relative position of
the fine cellulose fiber layer 12 and the hydrophobic non-woven
fabric layer 14 of the highly air-permeable and water-resistance
sheet.
[0249] [The Apertured Film]
[0250] The apertured film used as the buffer sheet in the absorbent
article according to the present invention is not limited so far as
it is a porous member having enough air permeability without
affecting the air permeability of the highly air-permeable and
water-resistance sheet. In addition, it is preferable that the
apertured film has a function which temporarily traps the liquid
such as body fluid not absorbed in the absorbent body. Further, the
apertured film is preferably of having a property which
fractionates and segmentalizes the liquid not absorbed in the
absorbent body and passed from the absorbent body. The material for
the apertured film having such a function includes homopolymer such
as polyethylene, polypropylene, polyethyleneterephthalate,
synthetic rubber, urethane and EVA, copolymer thereof, or
heteropolymer or of surface treated the forming body with these
materials using water repellant such as silicone and Teflon
(trademark) for enhancing the hydrophobicity. FIG. 11 is a
schematic view showing one of examples of the apertured film in the
present invention.
[0251] The pore size of the apertured film is preferably in the
range of 1 mm or lower, more preferably in the range of 0.5 mm or
lower. The thickness of the apertured film may be appropriately
changed in accordance with the thickness of the absorbent article.
In case of 1 mm or lower of the thickness of the absorbent body,
the thickness of the apertured film is preferably in the range of 3
mm or lower, more preferably in the range of 1 mm or lower. It
should be noted that, in order to stably provide the
above-mentioned cushioning characteristics, the apertured film may
be used of having high rigidity such that it does not greatly
change its shape under the load. In addition, the apertured film
may be of having a property which restores the bulk by absorbing
the moisture and water, along with maintaining the thin state at 1
mm or lower of thickness by compression deformation prior to the
use in the dry state.
[0252] In addition, the apertured film may be plastic film which is
formed to have a plurality of convex and concave portions, and of a
structure having a plurality of continuous cells like foam, in view
of fractionation and segmentalization of the passage of the liquid.
Typical example thereof includes urethane foam sheet having
continuous cell and plastic apertured film having convex and
concave structure.
[0253] The buffer sheet may be positioned in the almost whole
surface of the highly air-permeable and water-resistance sheet as
the backsheet, or in consideration of the cost, may be partially
positioned in a portion exposed a large amount of body fluid. For
example, the buffer sheet may be partially positioned in a portion
loaded the weight such as gluteal portion. When the surface area of
the buffer sheet is assigned as P, and the surface area of the
highly air-permeable and water-resistance sheet is assigned as Q,
the buffer sheet is preferably positioned such that P/Q.times.100
is in the range of 10 to 50%, more preferably in the range of 10 to
30%. In case of less than 10%, the passage of the liquid such as
body fluid is sometimes adequately enough fractionated and
segmentalized. In addition, in case of more than 50%, the cost is
disadvantage.
[0254] The absorbent article according to the present invention is
an absorbent article in which the above-mentioned highly
air-permeable and water-resistance sheet is used in the leakage
preventing material such as the backsheet. The absorbent article
according to the present invention includes disposable diaper and
women's sanitary product. The leakage preventing material
collectively refers to a member which is positioned at the
non-contact surface of the body of wearer as shown in FIG. 13.
[0255] The absorbent article according to the present invention
will be explained as one of examples for disposable diaper.
[0256] FIG. 12 is a deployed plan view of a disposable diaper, one
of examples of the absorbent article according to the present
invention. In addition, FIG. 13 is a cross-sectional view of FIG.
12 taken in line A-B.
[0257] As shown in FIGS. 12 and 13, an absorbent article 100 such
as disposable diaper comprises an connecting part 142 for wearing
the absorbent article 100 on the body, and an connected part 144
for locking the connecting part 142.
[0258] The absorbent article 100 mainly comprises a top sheet 122
consisting of liquid permeable non-woven fabric provided in the
contact surface of the body; a leakage preventing material 110
provided in the outer side at wearing; an absorbent body 116
interposed between the top sheet 122 and the leakage preventing
material 110; a leg gather 128 provided at both sides of the
absorbent body 116 on the top sheet 122 in the longitudinal
direction of the absorbent article 100; and a projecting part 136
provided in the inner side of the width direction of the absorbent
article 100 than the leg gather 128 along with the longitudinal
direction of the absorbent article 100.
[0259] The highly air-permeable and water-resistance sheet
according to the present invention is used as the leakage
preventing material 110 which is disposed in the outer side at
wearing without contacting with the body in the absorbent article
(disposable diaper) as mentioned above.
[0260] By using the highly air-permeable and water-resistance sheet
according to the present invention as the leakage preventing
material of the absorbent article, the absorbent article can be
obtained wherein the absorbent article does scarcely not occurred
to be stuffy of the skin and rash, since it has enough air
permeability, and the moisture such as urine is hardly leaked from
the absorbent article, since it has enough water resistance.
[0261] In addition, the absorbent article according to the present
invention may be the aspect as shown in FIGS. 14A to 14D. FIG. 14A
shows a development view of the absorbent article according to one
of aspects of the present invention, FIG. 14B is a cross-sectional
view of FIG. 14A along with line X-X', FIG. 14C is a
cross-sectional view of FIG. 14A along with line Y-Y', and FIG. 14D
is a schematic diagram of the absorbent article according to one
aspect of the present invention.
[0262] The absorbent article according to the present invention
comprises a first leakage preventing body 112 which is the
above-mentioned highly air-permeable and water-resistance sheet
according to the present invention at the outer surface of the
absorbent article, as shown in FIG. 14A. In the absorbent article,
a second leakage preventing body 114 which is the highly
air-permeable and water-resistance sheet according to the present
invention may be provided in the non-contact portion with the
wearer. In addition, the absorbent article according to the present
invention comprises a absorbent body 116 between the wearer and the
first leakage preventing body 112. Any members may be provided in
the absorbent article according to the present invention, the
members including a top sheet 122 having a liquid permeability, and
a leg gather 128, a bridge member 124 and a leg gather 130 for
holding the relative positional relationship between the wearer and
the absorbent article. It should be noted that notation 134
indicates a slit for positionally adjusting it to the excretion
organ of the wearer; notation 132 indicates a connecting part for
wearing the absorbent article to the wearer; notation P indicates a
urine receiving part which is one of portions of the absorbent body
116 and in which the liquid such as urine is contact with the
surface of the absorbent body; notation Q indicates which is one of
portions of the absorbent body 116 and in which the excretions such
as feces is received in the surface of the absorbent body; notation
LH indicates a leg hole for positioning it on the thigh of the
wearer; and notation W indicates a waist hole for positioning it
around the torso of the wearer.
EMBODIMENTS
Reference Example 1
[0263] The degassing step of the hydrophobic non-woven fabric layer
and the fine cellulose fiber layer layering step in which the fine
cellulose fiber layer is layered on the degassed hydrophobic
non-woven fabric layer has been examined with the following
materials and conditions.
[0264] [Materials and Conditions]
The hydrophobic non-woven fabric layer:
[0265] SMS (Weight:13 g/m.sup.2)
The degassing medium used in the degassing step:
[0266] Ethanol/Water=40/60
The clearance performing the degassing step:
[0267] 0.125 mm
The fine cellulose fiber:
[0268] MFC which is prepared from LDKP (wood pulp as prepared from
a smaller amount of broad leaf tree
The solvent used in the slurry of the fine cellulose fiber:
[0269] Ethanol/Water=50/50
The concentration of the fine cellulose fiber in the slurry:
[0270] 0.6 weight %
[0271] First degassing step was performed to the above-mentioned
hydrophobic non-woven fabric layer using 50 mL of the degassing
medium, and then second degassing step was performed using 40 mL of
the degassing medium. The fine cellulose fiber layer layering step
was performed in which 130 mL of the slurry of the fine cellulose
fiber is coated on the degassed hydrophobic non-woven fabric layer
by hand coating method at 1.20 mm, 1.00 mm and 0.75 mm of the
clearance of the coating. As the result, the obtained fine
cellulose fiber layers were uniform. It should be noted that the
weight per unit areas of the fine cellulose fiber layer (g/m.sup.2)
were 8.4, 7.8 and 6.5.
Reference Example 2
[0272] The Reference example 2 was performed in accordance with the
Reference example 1, except that the degassing medium used in the
degassing step was changed to 100% of Ethanol, the volumes of the
degassing medium used in the first and second degassing steps were
changed to 50 mL, respectively, the solvent used in the slurry of
the fine cellulose fiber was changed to water, and the fine
cellulose fiber layer layering step is performed along with the
full length of the hydrophobic non-woven fabric layer. As the
result, the agglomerate of MFC was disposed on SMS in the island
form, and it was of non-uniform.
Reference Example 3
[0273] The Reference example 3 was performed in accordance with the
Reference example 1, except that the degassing medium used in the
degassing step was changed to an aqueous solution containing LAS,
and the solvent used in the slurry of the fine cellulose fiber was
changed to water. As the result, the obtained fine cellulose fiber
layers were uniform. It should be noted that the weight per unit
area of the fine cellulose fiber layer (g/m.sup.2) was about 7.4,
respectively.
Reference Example 4
[0274] The Reference example 4 was performed in accordance with the
Reference example 1, except that the degassing medium used in the
degassing step was changed to 200 ppm and 400 ppm of an aqueous
solution of polyoxyethylene (10)/nonylphenyl ether (NPEO), and the
volumes of the degassing medium used in the first and second
degassing steps were changed to 50 mL, respectively. As the result,
the obtained fine cellulose fiber layers were uniform. It should be
noted that the weights per unit area of the fine cellulose fiber
layers (g/m.sup.2) were 5.7 and 7.9, respectively. In addition, the
speeds of permeating the degassing medium into the hydrophobic
non-woven fabric layer in the degassing step were rapid and slow,
respectively.
Reference Example 5
[0275] The Reference example 5 was performed in accordance with the
Reference example 4, except that the degassing medium used in the
first degassing step was changed in 400 ppm of an aqueous solution
of polyoxyethylene (10)/nonylphenyl ether (NPEO) and that in the
second degassing step was changed in 50 mL of water. As the result,
the obtained fine cellulose fiber layers were uniform. It should be
noted that the weights per unit area of the fine cellulose fiber
layers (g/m.sup.2) were about 7.9, respectively.
Embodiment 1
Preparation of MFC to be Tested
[0276] 267 kg of wood pulp originated from broad leaf tree (St.
Croix, Bonster) and 5 m.sup.3 of demineralized water were
introduced in 8.6 ton pulper to prepare 5% of pulp diluted
solution. This solution was processed in accordance with the
following process disclosed in Patent-related Document 4 using an
apparatus connected with 2 of DDRs (Double Disk Refiner, AIKAWA
Iron Works Co. Ltd.) at 1 m.sup.3/minute for 60 cycles to prepare
3.5% of MFC to be tested.
[0277] The hydration capacity: 30 mL/g
[0278] The average length of the fiber: 0.15 mm
[0279] The viscosity of 0.5% water dispersion liquid: [0280] 320
mPas
[0281] The above-mentioned process is as follows. That is, the
above-mentioned 5% of the diluted pulp solution was passed though
the apparatus connected in line-straight with 2 of DDRs by AIKAWA
Iron Works Co. Ltd. at 1 m.sup.3/minute to prepare MFC. [0282] Type
of DDR:AWR-14 [0283] Disk plate as used [0284] Teeth width: 2.0 mm
[0285] Groove width: 3.0 mm [0286] Clearance between the Disks as
used [0287] 0.15 to 0.25 mm
[0288] The MFC to be tested having the above-mentioned property was
obtained by means of passing through the DDR for 50 times with
checking its property every ten times. It should be noted that the
pulp concentration before the treatment was 5%, and the final
concentration was 3.5%, since it has diluted with the sealed
water.
[0289] <Preparation of MFC Slurry>
[0290] 90% of Ethanol was added to the MFC to be tested to prepare
the MFC slurry containing Ethanol/Water=50/50 (weigh ratio) having
0.7% of MFC concentration. The slurry was stored in the tank for
single purpose (not shown in the Drawing) until usage.
[0291] <The Substrate>
[0292] SMS made from polypropylene (Avgol) having the following
property was used.
[0293] Weight of SMS: 18 g/m.sup.2
[0294] Compositions of SMS: [0295] spun bond (1) (6.5/m.sup.2,
apparent denier::2.2) [0296] melt blown (5.0/m.sup.2, apparent
denier:0.5 or less) [0297] spun bond (2) (6.5/m.sup.2, apparent
denier::2.2)
[0298] Water resistance: 150 mmH.sub.2O
[0299] The substrate (Width: 1,500 mm, length: 10,000 m) was
disposed in the unreeler 232 as shown in FIG. 4A. It should be
noted that the substrate is supplied on the net conveyer 210 to be
set through the roller 222, and transferred to the reeler (not
shown in the Figure), in accordance with the Flowchart as shown in
FIG. 3A.
[0300] <The Saturation Medium>
[0301] A mixture of ethanol and water (mixing ratio=50/50 (volume)
was used as the saturation medium.
[0302] <Preparation of Layered Product of Hydrophobic Non-Woven
Fabric Layer/Fine Cellulose Fiber Layer>
[0303] The preparation was performed with the apparatus for
manufacturing as shown in FIG. 4A. First, the saturation medium was
supplied from the saturation medium supplier 214 at 1 ton/hour on
the moving substrate (sheet) at 40 m/minutes of the moving speed on
the net conveyer 210 to pretreat the substrate. The so supplied
saturation medium is supplied a narrow portion of the coater head
along with the movement of the substrate. It should be noted that
the gap (clearance) between the coating roller 220 and the net
conveyer 210 was set to 750 .mu.m by the height adjusting apparatus
(not shown in the Figure).
[0304] On the other hand, the coating slurry 202 is supplied from
the stored tank (not shown in the Figure) through the pipe and the
pump (not shown in the Figure) to the head box 212 such that the
liquid level of the slurry at the head box 212 is 60 mm. After the
pretreatment was finished, the supplied coating slurry 202 was
supplied on the above-mentioned substrate (sheet) at 2.5
ton/minutes of the ratio to form the fine cellulose fiber layer
(coating layer) on the substrate (sheet).
[0305] Next, this was supplied on the upper portion of an vacuum
unit 234, and removed the liquid at -30 kPa gauge, dried with the
drum type hot air drier (not shown in the Figure, set at about
100.degree.), and reeled to obtain the layered product of the
hydrophobic non-woven fabric layer/fine cellulose fiber layer. It
should be noted that the efficiency of the layered product of the
hydrophobic non-woven fabric layer/fine cellulose fiber layer is as
follows.
[0306] Weight: 26.0 g/m.sup.2 [0307] The hydrophobic non-woven
fabric: 18.0 g/m.sup.2 [0308] MFC coating: 8.0 g/m.sup.2
[0309] Water pressure resistance: [0310] 400 mmH.sub.2O
[0311] As the result, it was found that the water pressure
resistance of the layered product of the hydrophobic non-woven
fabric layer/fine cellulose fiber layer (400 mmH.sub.2O) is greatly
improved in comparison with the water pressure resistance of the
hydrophobic non-woven fabric layer (150 mmH.sub.2O).
[0312] The so obtained layered product of the hydrophobic non-woven
fabric layer/fine cellulose fiber layer (A4 size) was immersed in
the 10 w/v % methylhydrogen silicone oil of solvent diluted
solution in which methylhydrogen silicone oil (TSF484, Toshiba
silicone) is diluted with N-hexane for 1 minute. This was air dried
in the state which is sandwiched with filter paper to dry. It
should be noted that the adsorbed amount of the methylhydrogen
silicone oil to the layered product was 2 g/m.sup.2. Then this was
heat treated for 60 minutes at 150 to obtain a highly air-permeable
and water-resistance sheet 1 according to the present invention.
The following examination was performed with regard to the highly
air-permeable and water-resistance sheet. The result was shown as
follows.
[0313] The weigh of the composite sheet (average): [0314] 26.0
g/m.sup.2
[0315] The weigh of the highly air-permeable and water-resistance
sheet (average): [0316] 28.3 g/m.sup.2
[0317] The adsorbed amount of the water repellant layer: [0318] 2.3
g
[0319] Water pressure resistance: [0320] 565 mmH.sub.2O
[0321] Air permeability in accordance with Gurley method: [0322] 6
seconds
Embodiment 2
[0323] The Embodiment 2 was performed in accordance with the
Embodiment 1, except that the apparatus as shown in 4A was changed
to an apparatus having precoat bath as shown in FIG. 6, water is
used as the saturation medium, the substrate (sheet) was
transferred in a state that the saturation medium is dropped on the
hydrophobic non-woven fabric layer of the sheet 200 from the porous
plate of the head box 212 to accumulate the water liquid, so as to
form the fine cellulose fiber layer (coating layer) on the
substrate (sheet).
[0324] Next, this was supplied to the upper portion of the vacuum
unit (as the same as shown in FIG. 4A) to remove the liquid at -30
kPa gauge.
[0325] Further, the water repellant treatment was treated as
follows, then dewatered by vacuum. After that, it was dried under
heat at 120.degree., and surface treated with the cylinder roll
having 150.degree. of surface temperature to obtain a highly
air-permeable and water-resistance sheet 2.
[0326] That is, 30 g (solid content)/L of a treatment solution (100
L) comprising the following water repellant PA-1 and water was used
in the water repellant treatment.
[0327] <Water Repellant PA-1 (AOKI OIL INDUSTRIAL CO.,
LTD.)>
[0328] Composition: [0329] A product in which the paraffin wax
water repellant was combined with melamine resin
[0330] Appearance: [0331] o/w Yellow emulsion with light yellow
[0332] Ionic character: [0333] Anionic
[0334] pH: 9.0
[0335] Concentration of the solid content: [0336] 30%
[0337] The treatment solution was dropped on the cellulose fiber
layer at 15 mL/minute from the batch equipped in zigzag form with a
porous plate having 0.7 mm diameter of pore on the rectangular
bottom of the bath such that the water repellant is mainly remained
on the cellulose fiber layer, and removed the liquid at -20 MPa
gauge. It should be noted that the removed solution was recycled to
be used.
[0338] With regard to the highly air-permeable and water-resistance
sheet 2, the following examinations were performed. The result is
shown as follows.
[0339] The weight of the hydrophobic non-woven fabric layer: [0340]
18.0 g/m.sup.2
[0341] The weight of the MFC coating: [0342] 8.0 g/m.sup.2
[0343] The adsorbed amount of PA-1: [0344] 5.0 g/m.sup.2
[0345] Water pressure resistance: [0346] 488 mmH.sub.2O
[0347] The contact angle of the water liquid: [0348] 99.degree.
[0349] Water absorbent ratio in water: [0350] 1.4% (for 2
hours)
[0351] (It should be noted that the "water absorbent ratio in
water" means a percentage which corresponds to the increase in
weight of the highly air permeability water resistance sheet before
and after the immersion wherein the increase is calculated such
that the highly are permeability water resistance sheet to be
weighted is sandwiched with the stainless net, and it is immersed
in the ion exchanged water for 2 hours.)
[0352] The air permeability in accordance with Gurley method:
[0353] 8 seconds
[0354] It should be noted that the highly air permeability and
water resistance sheet is subjected to the delamination test in
which the sheet after the calendering process is twisted for 10
times by hand. As the result, the delamination of the sheet was not
occurred and stabled. It was considered that MFC of the fine
cellulose fiber layer is incorporated into the hydrophobic
non-woven fabric layer and the sheet is in the state as shown in
FIG. 1b.
Embodiment 3
[0355] It was manufactured to use the highly air-permeable and
water-resistance sheet 2 of the Embodiment 2 as a first leakage
preventing body 112 and a second leakage preventing body 114 as
shown in FIGS. 14A to 14D of the diaper for child. In addition, in
the absorbent article 100, the coating patter and structure of the
absorbent body (Shanghai DSG Megathin, an absorbent body in the
sheet form) as shown in FIGS. 15A to 15B having the following
efficiency were used in the absorbent body 116.
[0356] The weight of SAP: [0357] 200 g/m.sup.2
[0358] The weight of the substrate: [0359] 40 g/m.sup.2
[0360] The weight of the absorbent body: [0361] 240 g/m.sup.2
[0362] The content of SAP in the absorbent body: [0363] 86%
[0364] The air permeability of the absorbent body: [0365] 4 seconds
(Gurley method)
[0366] The content, designed free absorbing amount and designed
dewatered absorbing amount of SAP of the absorbent body used in the
absorbent article 100 are shown in Table 1.
TABLE-US-00001 TABLE 1 Volume to be designed Amount of Weight of
Amount of desorbing and absorbent body absorbing water retaining
water (g) (mL) (mL) 10.0 500 300 (as SAP)
[0367] <The Air Permeability of the Absorbent Article
100>
[0368] The air permeability according to the Gurley method of the
absorbent article 100 in the extended state was examined in the
[0369] As the result, it was found that the permeability was in the
range of 6 to 10 second, and the article has a large air
permeability as the diaper product.
[0370] <Result of the Wearing Test>
[0371] 4 of the absorbent article per a baby were worn on 6 wearers
of 3 male babies and 3 girl babies having normal excretion
mechanism. The parent of the wearer was asked to recode dairy
report indicating its use, and all of the diapers after use were
retrieved and analyzed. With regard to the main posture of the
wearer, the average wearing time, stuffy and rash and the absorbent
article after use, the average amounts of urine and feces and
number of the diaper as leaked is shown in Table 2. It should be
noted that the normal wearing time of the diaper is around 3
hours.
TABLE-US-00002 TABLE 2 Amount of Number of Wearing Wearing Stuffy
absorption Numbre of use excreting feces Number of leakage posture
time and rush (average g) (use/total) (number/use) Urine Feces
Upright, Sitting, 5.5 no 205 13/24 10/13 0/13 1/10 Walk, Clawling,
and Face-down Dorsal and recumbent 7.5 no 220 11/24 5/11 1/11 0/5
position Average 6.4 221 Number of usage Number of usage Total
number of Total number of for urine 24 for feces 15 urine leakage
1/24 feces leakage 1/15
[0372] Although it was used for a long time, and almost of the
wearers excreted both of urine and feces, it was not stuffy, the
rash was not occurred, and the leakage was extremely less, and the
good result was obtained.
Embodiment 4
[0373] The highly air-permeable and water-resistance sheet as
obtained in the Embodiment 2 were used as the highly air-permeable
and water-resistance sheet according to the present invention. The
highly air-permeable and water-resistance sheet was disposed in the
backsheet of the child diaper commercially available (Product Name:
"Muni Nobi-ru fit" (Unicharm)) in accordance with the following
procedure. The application effect of the child diaper was
examined.
[0374] <Method for Disposing the Highly Air-Permeable and
Water-Resistance Sheet According to the Present Invention>
[0375] The backsheet (the laminate of the air permeable film and
the non-woven fabric) of the above-mentioned child diaper were cut
with the sized of 130 mm width and 355 mm length from the backsheet
side as shown in FIG. 16 to form an window. The highly
air-permeable and water-resistance sheet 2 (170 mm width, 390 mm
length) according to the present invention as obtained in the
Embodiment 2 was connected to the window with two types of
double-faced tape (one of tape having core and the other having
no-core) so as not to occur any leakage, thereby manufacturing a
diaper 1 to be examined.
[0376] <Use Test by Babies>
[0377] The above-mentioned diaper to be examined was worn on 8
babies (4 male babies and 4 girl babies). The leakage stability
from the diaper and the backsheet was examined in accordance with
the above-mentioned <Result of the wearing test>. It should
be noted that the wearing time was set for 3 hours at average. The
result is shown in Table 3.
TABLE-US-00003 TABLE 3 Number of Number of use leakage Leakage from
backsheet 40 3 35: There is no leakage from (Feces: 1 backsheet
Urine: 2) 3: Bleeding in the circular form at the rear portion 2:
Bleeding in the pinhole form (1: no leakage)
Embodiment 5
[0378] A diaper to be examined was manufactured with the same
method for disposing in accordance with the same type of the diaper
as shown in the Embodiment 4. That is, the highly air-permeable and
water-resistance sheet 2 as obtained in the Embodiment 2 as the
highly air-permeable and water-resistance sheet according to the
present invention was disposed and an apertured film as the buffer
sheet as the buffer sheet was disposed at the water resistance
hydrophobic non-woven fabric layer side of the highly air-permeable
and water-resistance sheet 2 to manufacture a diaper 2 to be
examined.
[0379] With regard to the diaper to be examined (as used for 5
diapers per a baby), the leakage stability was examined in
accordance with the above-mentioned <Result of the wearing
test>. It should be noted that the wearing time are set as 6
hours (night) at average. The result is shown in Table 4.
TABLE-US-00004 TABLE 4 Number of Number of use leakage Leakage from
backsheet 40 7 39: There is no leakage from (Feces: 1 backsheet
Urine: 6) 1: Bleeding in the pinhole form as observed
[0380] Although the same highly air-permeable and water-resistance
sheet as that of the Embodiment 4 was used, it was confirmed that
the leakage stability from the backsheet is improved in comparison
with the Embodiment 4.
Embodiment 6
[0381] MFC was prepared as follows.
[0382] First, the craft pulp originated from broad leaf tree
(Dai-showa/Marubeni international Co. Ltd., Product name: piece
liver LBKP) was defiberized in the pulper at 5 weight % of the
concentration, transferred to the recycle tank, and prepared 3.5
weight % of the concentration. 3.5 weight % of the pulp slurry was
beated with double disk refiner (hereinafter, referred to as DDR)
in accordance with the following condition to prepare MFC. The
condition was as follows. That is, the load was applied as possible
such that the metal thereof is not contact with each other (Contact
of the fixed blade with the rotating blade).
[0383] DDR machine: [0384] AW14 made by AIKAWA Iron Works Co.
Ltd.
[0385] Disk plate: [0386] blade width 2.0 mm, groove width 3.0
mm
[0387] Flow rate of the pulp to DDR: [0388] 1 m.sup.2/minute
[0389] Number of times passed though DDR: [0390] 100
[0391] Clearance of the blade: [0392] 0.23 to 0.13 mm
[0393] The property of MFC as prepared was as follows.
[0394] The hydration capacity: [0395] 27 mL/g
[0396] The average fiber length: [0397] 0.15 mm
[0398] The viscosity of 0.5 weight % of the slurry [0399] 320
mPas
[0400] The final concentration: [0401] 3.0 weight % (diluted with
the seal water)
[0402] <Preparation of MFC Slurry>
[0403] Ethanol was added to MFC as mentioned above to prepare the
MFC slurry containing Ethanol/Water=65/35 (weigh ratio) having 0.7%
of MFC concentration.
[0404] <The Non-Woven Fabric>
[0405] SMS non-woven fabric made from polypropylene (AVGOL) having
the following property was used
[0406] The weight: 15 g/m.sup.2
[0407] Constitution of SMS: [0408] spun bond (1) (5.0 g/m.sup.2)
[0409] melt blown (5.0 g/m.sup.2) [0410] spun bond (2) (5.0
g/m.sup.2)
[0411] The water pressure resistance: 150 mmH.sub.2O
[0412] <Coating of the MFC Slurry to the Non-Woven
Fabric>
[0413] The above-mentioned non-woven fabric (width 1,500 mm, length
10,000 mm) was disposed on the unreeler 232 as shown in FIG. 4A.
The non-woven fabric was supplied on the net conveyer 210 through
the roller 222. Water was supplied from the saturation medium
supplier 214 at 17 kg/hour on the moving non-woven fabric at 40
m/minutes of the moving speed on the net conveyer 210 to be
subjected to pretreatment of saturating the non-woven fabric with
water. The so supplied saturation medium comprising water was
coated at the narrow portion of the coater head along with the
movement of the non-woven fabric. It should be noted that the
clearance between the coating roller 220 and the net conveyer 210
was set to 750 .mu.m by the height adjusting apparatus. On the
other hand, the coating slurry 202 is supplied from the storage
tank such that the liquid level in the head box 212 is 60 mm. After
the above-mentioned pretreatment is finished, the supplied coating
slurry 202 was supplied to the above-mentioned non-woven fabric at
42 kg/minute to form the fine cellulose fiber layer on the
non-woven fabric.
[0414] Next, this was supplied to the upper portion of the vacuum
unit 234, was removed the liquid with vacuum at -30 kPa, dried at
100.degree. C. with the cylinder drier, and reeled to obtain the
composite sheet. In this apparatus, ethanol in the drainages of the
removed part and of drier part was recovered with a solvent
recovering apparatus (not shown in the Figure), and recycled. So,
the drier part is completely sealed and is filled up with nitrogen
gas to prevent the flash and combustion of ethanol. It should be
noted that the property of the composite sheet is as follows. As
the result, it was confirmed that the water pressure resistance of
the composite sheet (400 mmH.sub.2O) is greatly improved in
comparison with the water pressure resistance of the non-woven
fabric (150 mmH.sub.2O).
[0415] Weight: 20 g/m.sup.2(SMS: 15 g/m.sup.2, MFC: 5
g/m.sup.2)
[0416] Water pressure resistance: 400 mmH.sub.2O
[0417] <Preparation of Coating Composition for the Water
Repellant Layer>
[0418] 50 weight parts of the olefinic water repellent (Meisei
Chemical Works Ltd., Product name: Petrox P300) and 48 weight parts
of stylene butadiene resin (Nippon A&L Inc., Product name:
Smartex PA3802) were mixed under stirring to prepare a main agent.
Then, prior to performing the coating, 2 weight parts of zirconium
carbonate cross linker (Nippon Light Metal Co. Ltd., Product name:
Bay coat 20) was added to the main agent, and water was added to
prepare the coating composition having 40 weight % of the solid
content. At that time, the viscosity of the coating composition was
95 mPas, and was 17 seconds in accordance with Zahn cup method.
[0419] The nature of the olefinic water repellent, stylene
butadiene resin and the zirconium carbonate cross linker are as
follows.
[0420] (The Olefinic Water Repellent)
[0421] Composition: wax type emulsion (Meisei Chemical Works Ltd.,
Product name: Petrox P300)
[0422] Appearance: white liquid
[0423] pH: 8.5
[0424] Ionic character: Nonion
[0425] Concentration of the solid content: [0426] 34 weight %
[0427] (The Stylene Butadiene Resin)
[0428] Composition: [0429] stylene/butadiene ratex [0430] (Nippon
A&L Inc., Product name: Smartex PA3802)
[0431] Monomer composition: [0432] butadiene 30, stylene 59, MMA 3,
CAN 5, acid 3
[0433] Tg: 21.degree. C.
[0434] Average particle diameter: [0435] 200 nm
[0436] Appearance: [0437] white liquid
[0438] pH: 6.1
[0439] Ionic character: [0440] Anionic
[0441] Concentration of the solid content: [0442] 48 weight %
[0443] (The Zirconium Carbonate Cross Linker)
[0444] Composition: [0445] ammonia zirconium carbonate [0446]
(Nippon Light Metal Co. Ltd., Product name: Bay coat 20)
[0447] Chemical formula:
(NH.sub.4).sub.2[Zr(CO.sub.3).sub.2(OH).sub.2]
[0448] Appearance: [0449] white liquid
[0450] pH: 9.0-9.5
[0451] Ionic character: [0452] Anionic
[0453] Concentration of the solid content: [0454] 20 weight %
[0455] <Preparation of the Highly Air-Permeable and
Water-Resistance Sheet with the Coating of the Water Repellant
Layer>
[0456] The coating composition for the water repellant layer was
coated on the side of the fine cellulose fiber layer of the
composite sheet as obtained with flexographic coater in accordance
with the following condition. The amount of the coating was 2.1
g/m.sup.2.
[0457] Aniolox roll: [0458] 130 lines
[0459] Coating speed: [0460] 100 g/minute
[0461] Dry temperature of the air drier: [0462] 100.degree. C.
[0463] After the coating, the heat press treatment was performed
(linear pressure: 100 kg/cm). Then, it was processed at 120.degree.
C. for 30 minutes in the drier to prepare the highly air-permeable
and water-resistance sheet according to the present invention.
[0464] [Effect of the Heat Press Treatment]
[0465] The properties before and after the heat press treatment are
shown in Table 5. The thickness is reduced to 2/3 or lower by
pressing in comparison with the prior to the treatment, and the
treatment has an effect that products using the highly
air-permeable and water-resistance sheet does not become bulky. In
addition, the smoothness was improved from 1 second to 5 seconds.
Accordingly, it is possible to print finer picture. It should be
noted that "smoothness [coating side]" means a smoothness of the
surface of the water repellant layer as layered on the non-woven
fabric by the coating, and "smoothness [non-coating side]" means a
smoothness of the opposite surface.
TABLE-US-00005 TABLE 5 Before After heat press heat press treatment
treatment Thickness (.mu.m) 88 56 Air permeability 1 2 by Gurley
method (S/100 mL) Smoothness[coating side] (s) 1 5 Smoothness 1 2
[Non-coating side] (s)
[0466] The result of the property for this highly air-permeable and
water-resistance sheet as measured is shown as follows.
[0467] The weight of the SMS non-woven fabric: [0468] 15
g/m.sup.2
[0469] The weight of MFC: [0470] 5 g/m.sup.2
[0471] The coating amount of the water repellant layer: [0472] 2.1
g/m.sup.2
[0473] The water repellency (JIS P8137): [0474] R10
[0475] The water pressure resistance: [0476] 488 mmH.sub.2O
[0477] The air permeability by Gurley method: [0478] 2 seconds/100
mL
Embodiment 7
[0479] The highly air-permeable and water-resistance sheet was
obtained in accordance with the Embodiment 6, except that the water
repellant layer is changed as follows, and the coating amount of
the water repellant layer to the composite sheet is changed to 2.0
g/m.sup.2.
[0480] <Preparation of the Coating Composition for the Water
Repellant Layer>
[0481] 50 weight parts of the olefinic water repellent (Meisei
Chemical Works Ltd., Product name: Petrox P300) and 48 weight parts
of stylene butadiene resin (Nippon A&L Inc., Product name:
Smartex PA3802) was mixed under stirring to prepare a main agent.
Then, prior to performing the coating, 2 weight parts of polyamide
epichlorohydrin cross linker (Sumitomo Chemical Co. Ltd., Product
name: Sumirez resin SPI-203) was added to the main agent, and water
was added to prepare 40 weight % of the coating composition. At
that time, the viscosity of the coating composition was 95 mPas,
and was 17 seconds in accordance with Zahn cup method.
[0482] The property of the polyamide epichlorohydrin cross linker
(Sumitomo Chemical Co. Ltd., Product name: Sumirez resin SPI-203)
is as follows.
[0483] Composition: [0484] polyamide epichlorohydrin
[0485] Appearance: [0486] clear liquid, Colorless-light yellow
[0487] pH: 6.0 to 8.0
[0488] Ionic character: [0489] Cation
[0490] Concentration of the solid content: [0491] 50 weight %
Comparative Example 1
[0492] The composite sheet as obtained in the Embodiment 6 was
subjected to the heat press treatment (linear pressure: 100 kg/cm)
to obtain a sheet for comparison not coated with the water
repellant layer.
Comparative Example 2
[0493] The silicone water repellant layer (Shin-Etsu Chemical Co.
Ltd., Product name: POLON NWS) was only coated to the composite
sheet as obtained in the Embodiment 6 as follows to obtain a sheet
for comparison. It should be noted that the property of the
silicone water repellant layer (Shin-Etsu Chemical Co. Ltd.,
Product name: POLON NWS) is as follows.
[0494] Composition: [0495] silicone emulsion
[0496] Appearance: [0497] White liquid
[0498] Ionic character: [0499] Anion
[0500] Concentration of the solid content: [0501] 30 weight %
[0502] Coating of the Silicone Water Repellant Layer>
[0503] A coating composition in which the silicone water repellant
layer is diluted with water to the composition having 10 weight %
of the solid content was hand coated with the bar on the surface of
the fine cellulose fiber layer of the composite sheet to prepare a
sheet having 2.1 g/m.sup.2 of the coating amount. After the
coating, it was heated at 120.degree. C. for 30 minutes in the
drier, then subjected to the heat press treatment at 100 kg/cm of
the linear pressure.
Comparative Example 3
[0504] The fluorinated water and oil repellant (Solvay Solexis
K.K., Product name: Solvera PT5045) was only coated to the
composite sheet as obtained in the Embodiment 6 as follows to
obtain a sheet for comparison. It should be noted that the property
of the fluorinated water and oil repellant (Solvay Solexis K.K.,
Product name: Solvera PT5045) is as follows.
[0505] Composition: [0506] fluorinated dispersion
[0507] Appearance: [0508] clear solution with amber color
[0509] pH: [0510] 7 to 9
[0511] Concentration of the solid content: [0512] 20 weight %
[0513] Coating of the Fluorinated Water and Oil Repellant>
[0514] The coating composition in which the above-mentioned
fluorinated water and oil repellant is diluted with water to
prepare the composition having 10 weight % of the solid content was
hand coated to the side of the fine cellulose fiber layer of the
composite sheet with the bar to prepare a sheet having 2.2
g/m.sup.2 of the coating amount. After the coating, it was heated
at 120.degree. C. for 30 minutes, then subjected to the heat press
treatment at 100 kg/cm of the linear pressure.
Comparative Example 4
[0515] The olefinic water repellent (Meisei Chemical Works Ltd.,
Product name: Petrox P300) as used in the Embodiment 6 was only
coated to the composite sheet as obtained in the Embodiment 6 as
follows to obtain a sheet for comparison.
[0516] <Coating of the Olefinic Water Repellent>
[0517] A coating composition in which the above-mentioned olefinic
water repellent is diluted with water to the composition having 10
weight % of the solid content was hand coated with the bar on the
surface of the fine cellulose fiber layer of the composite sheet to
prepare a sheet having 2.0 g/m.sup.2 of the coating amount. After
the coating, it was heated at 120.degree. C. for 30 minutes the
drier, then subjected to the heat press treatment at 100 kg/cm of
the linear pressure.
Comparative Example 5
[0518] The water repellant layer was coated to the composite sheet
as obtained in the Embodiment 6 using the acrylate water repellant
to obtain a sheet for comparison.
[0519] <Preparation of the Coating Composition>
[0520] 50 weight parts of the acrylate water repellant (Saiden
Chemical Industry Co. Ltd., Product name: Saibinol EK-752) and 48
weight parts of the stylene butadiene resin (Nippon A&L Inc.,
Product name: Smartex PA3802) was mixed under stirring to prepare a
main agent. Then, prior to performing the coating, 2 weight parts
of polyamide epichlorohydrin cross linker (Sumitomo Chemical Co.
Ltd., Product name: Sumirez resin SPI-203) was added to the main
agent, and water was added to prepare 40 weight % of the coating
composition. At that time, the viscosity of the coating composition
was 95 mPas, and was 17 seconds in accordance with Zahn cup method.
It should be noted that the property of the acrylate water
repellant (Saiden Chemical Industry Co. Ltd., Product name:
Saibinol EK-752) is as follows.
[0521] Composition: [0522] acrylate polymer emulsion
[0523] Appearance: [0524] white liquid
[0525] pH: 8.0 to 9.0
[0526] Ionic character: [0527] Anion
[0528] Concentration of the solid content: [0529] 46 weight %
[0530] (Coating of the Coating Composition for the Water Repellant
Layer)
[0531] The coating composition for the water repellant layer was
coated to the side of the fine cellulose fiber layer of the
composite sheet with flexographic coater in accordance with the
following condition. At that time, the coating amount was 2.3
g/m.sup.2.
[0532] Aniolox roll: [0533] 130 lines
[0534] Coating speed: [0535] 100 g/minute
[0536] Dry temperature of the air drier: [0537] 100.degree. C.
[0538] After the coating, the heat press treatment was performed
(linear pressure: 100 kg/cm). Then, it was processed at 120.degree.
C. for 30 minutes in the drier to prepare a sheet for
comparison.
[0539] Next, with regard to the sheets as obtained in the
Embodiments 6 and 7 and Comparative examples 1 to 5, the following
air permeability was examined. The result is shown in Table 6.
[0540] As clearly shown Table 6, with regard the Embodiment 6, it
has low air permeability value after the heat press treatment, and
it is good air permeability. With regard to the Embodiment 7, the
air permeability is maintained in the good level, although the air
permeability after the heat press treatment is slightly bad due to
the difference of the cross linker. On the other hand, the air
permeability after the heat press treatment is almost the same of
the current backsheet (porous film), since the water repellant
layer of the Comparative example 5 is easy to form the film.
Accordingly, it has a practical problem.
TABLE-US-00006 TABLE 6 Air permeability Air permeability before
heat after heat press treatment press treatment (S/100 mL) (S/100
mL) Embodiment 6 1 2 Embodiment 7 5 20 Comparative example 1 1 1
Comparative example 2 1 1 Comparative example 3 1 1 Comparative
example 4 1 1 Comparative example 5 70 151
[0541] [The Water Resistance]
[0542] The water resistance test of the sheets as obtained in the
Embodiments 6 and 7 and the Comparative examples 1 to 5 was
performed as follows. That is, the sheet was disposed on the paper
filter, 10 wiper papers (Crecia Co. Ltd., Product name: Kim Towel)
containing enough amounts of water were disposed on the sheet, and
5 kg of the weight was further disposed thereon, and the leaked
water to the paper filter was observed.
[0543] The result of the water resistance test is shown in Table 7.
As clearly shown in Table 7, in the Embodiment 6, the leakage to
the paper filter was not observed until 5 hours, and the water
resistance is extremely good. In the Embodiment 7, the leakage was
not observed until 2 hours, the water resistance is relatively
good, although it is slightly bad. On the other hand, in the
Comparative example 1, the water was leaked after 1 minutes, and in
the Comparative examples 2 to 5, the water was leaked after 10 to
15 minutes. These sheets as obtained in the Comparative examples 1
to 5 have not enough water resistance. The condition of the water
resistance test is harder than the use condition of the backsheet
for the commercially available child diaper. So, even though the
highly air-permeable and water-resistance sheet according to the
present invention (Embodiments 6 and 7) is used for the backsheet
of the commercially available child diaper, there is no risk of the
leakage for long time, and it can stand the practical use.
TABLE-US-00007 TABLE 7 Leakage state to the paper filter Embodiment
6 No leakage after 5 hours Embodiment 7 Leakage after 2 hours in
the pinhole form Comparative example 1 Leakage after 1 minute
Comparative example 2 Leakage after 10 minutes Comparative example
3 Leakage after 10 minutes Comparative example 4 Leakage after 10
minutes Comparative example 5 Leakage after 15 minutes
Embodiment 8
[0544] An example will be described to confirm that the highly
air-permeable and water-resistance sheet as obtained in the
Embodiment 6 can be applied to the backsheet of the child diaper.
The backsheet of the commercially available child diaper was
replaced with the highly air-permeable and water-resistance sheet
according to the present invention to manufacture a diaper for
test. The wearing test was performed using the diaper for test to
the baby. As the test, the urine leakage, the skin to be stuffy and
the rush were observed after the predetermined period was passed
from the beginning of wearing.
[0545] <Preparation of the Diaper for Test>
[0546] The backsheet (laminate of the air permeable film and the
non-woven fabric) was removed from the child diaper as shown in
FIGS. 12 and 13 (Unicham Co. Ltd., Product name: Muni Nobi-ru fit)
by cold spraying the connecting part. The highly air-permeable and
water-resistance sheet according to the present invention was
disposed in the removed part of the diaper to prepare 40 of the
child diapers for test.
[0547] <The Wearing Test by Baby>
[0548] 40 of the child diapers for test were prepared, and it was
worn to 8 babies (4 male babies, and 4 girl babies) having normal
excretion mechanism (5 diapers per baby used). The parent of the
wearer was asked to recode dairy report indicating its use, all of
the diapers after use were retrieved, and the leakage from the
disposed highly air-permeable and water-resistance sheet according
to the present invention was confirmed. The wearing time was set
for 3 hours in average. As the result, any leakages from the
disposed highly air-permeable and water-resistance sheet according
to the present invention were not observed in 35 diapers among 40
diapers. In addition, the bleeding in the circular form was
observed at the rear part of the diaper was observed in 3 diapers,
and the bleeding in the pinhole form was observed in 2 diapers.
However, its degree of the bleeding is not problematic. In
addition, with regard to all of babies, there is no stuffy and
rush. It was confirmed from these results that the child diaper in
which the highly air-permeable and water-resistance sheet according
to the present invention is used for the backsheet can be
practically applicable.
Embodiment 9
[0549] 0.5 weight part of the dispersant (San Nopco Limited,
Product name: SN Dispersant) and water was added to 100 weight part
of zeolite originated from the natural origin (Nitto Funka Co.
Ltd., Product name: SP#2300), and dispersed with dispersing
apparatus for 20 minutes to prepare a homogeneous slurry of
deodorizer having 50 weight % of the solid content.
[0550] <Preparation of Mixed Coating Composition of the Water
Repellant Layer and Deodorizer>
[0551] 50 weight parts of the olefinic water repellent (Meisei
Chemical Works Ltd., Product name: Petrox P300) and 48 weight parts
of stylene butadiene resin (Nippon A&L Inc., Product name:
Smartex PA3802) were mixed with the slurry of the deodorizer under
stirring to prepare a main agent. Then, prior to performing the
coating, 2 weight parts of zirconium carbonate cross linker (Nippon
Light Metal Co. Ltd., Product name: Bay coat 20) was added to the
main agent, and water was added to prepare 40 weight % of the
coating composition having 40 weight % of the all solid contents.
At that time, the viscosity of the coating composition was 95
mPas.
[0552] The property of zeolite originated from the natural
resources as used in the Embodiment is as follows. It should be
noted that the nature of the olefinic water repellent, stylene
butadiene resin and zirconium carbonate cross linker are as
follows.
[0553] (The Zeolite Originated from Natural Resources)
[0554] Composition: [0555] zeolite originated from natural
resources
[0555] (Ca,K.sub.2,Na.sub.2){AlSi.sub.5O.sub.12}.sub.27H.sub.2O
[0556] (Nitto Funka Co. Ltd., Product name: SP#2300)
[0557] Crystal structure: [0558] mordenite
[0559] pH: 6.4
[0560] Base exchange capacity: [0561] 160 to 190 meq/100 g
[0562] Moisture: [0563] 7.4%
[0564] Whiteness: [0565] 60%
[0566] Preparation of the Highly Air-Permeable and Water-Resistance
Sheet by Coating the Mixed Coating Composition of the Water
Repellant Layer and the Deodorizer
[0567] The mixed coating composition of the water repellant layer
and the deodorizer was coated on the side of the fine cellulose
fiber layer of the composite sheet as obtained using the bar in
accordance with the mayerbar method.
[0568] The bar as used: 0.15 mm
[0569] Dry temperature: 110.degree. C. for 2 minutes
[0570] After the coating, the heat press treatment was performed,
then it was heated at 120.degree. C. for 30 minutes to prepare the
highly air-permeable and water-resistance sheet according to the
present invention.
[0571] Linear pressure for the heat press treatment: [0572] 100
kg/cm
[0573] Speed of the heat press treatment: [0574] 10 m/minutes
[0575] Roll temperature: [0576] 30.degree. C.
[0577] The result of the property of the highly air-permeable and
water-resistance sheet as measured is shown as follows.
[0578] The weight of SMS non-woven fabric: [0579] 15 g/m.sup.2
[0580] The weight of MFC: [0581] 5 g/m.sup.2
[0582] The coating amount of the deodorizer [0583] 2.05
g/m.sup.2
[0584] The water repellency (JIS P8137): [0585] R10
[0586] The air permeability by Gurley method: [0587] 2 seconds/100
mL
Embodiment 10
[0588] The Embodiment 10 was performed in accordance with the
Embodiment 9, except that the deodorizer of zeolite originated from
the natural resources is changed to the deodorizer of the following
ultra fine white clay to obtain the highly air-permeable and
water-resistance sheet according to the present invention.
[0589] (The Deodorizer of Ultra Fine White Clay)
[0590] Component: [0591] Alumino silicate glass [0592] (Shirax Co.
Ltd., Product name: Shirax fine balloon SFB-101)
[0593] Composition: [0594] SiO.sub.2(69.about.73%),
Al.sub.2O.sub.3(12.about.13%)
[0595] Particle size: [0596] 20 .mu.m
[0597] Outer structure: [0598] Spherical
[0599] Inner structure: [0600] Honeycomb (a plurality of
barriers)
[0601] Particle density: [0602] 0.6 to 0.8
[0603] Bulk density: [0604] 0.23 to 0.32
[0605] Hunter whiteness: [0606] 80%
[0607] The result for the property of the manufactured highly
air-permeable and water-resistance sheet is shown as follows.
[0608] The weight of SMS non-woven fabric: [0609] 15 g/m.sup.2
[0610] The weight of MFC: [0611] 5 g/m.sup.2
[0612] The coating amount of the deodorizer [0613] 2.05
g/m.sup.2
[0614] The coating amount of the water repellant layer [0615] 2.05
g/m.sup.2
[0616] The water repellency (JIS P8137): [0617] R10
[0618] The air permeability by Gurley method: [0619] 6 seconds/100
mL
Embodiment 11
[0620] The Embodiment 11 was performed in accordance with the
Embodiment 9, except that the deodorizer of zeolite originated from
the natural resources is changed to the deodorizer of the following
synthetic zeolite to obtain the highly air-permeable and
water-resistance sheet according to the present invention.
[0621] (The Deodorizer of Ultra Fine White Clay)
[0622] Chemical name: [0623] Calcium A type zeolite [0624] (Nippon
chemical industrial Co. Ltd., Product name: Zeostar CA-110P)
[0625] Composition: [0626] CaO(13%), Al.sub.2O.sub.3(30%)
[0627] Particle size: [0628] 20 .mu.m
[0629] Outer structure: [0630] Horn shape
[0631] ignition loss: [0632] 4.1% (800.degree. C.)
[0633] pH: [0634] 11.5 (5% slurry, 20.degree. C.)
[0635] The result for the property of the highly air-permeable and
water-resistance sheet is shown as follows.
[0636] The weight of SMS non-woven fabric: [0637] 15 g/m.sup.2
[0638] The weight of MFC: [0639] 5 g/m.sup.2
[0640] The coating amount of the deodorizer [0641] 2.0
g/m.sup.2
[0642] The coating amount of the water repellant layer [0643] 2.0
g/m.sup.2
[0644] The water repellency (JIS P8137): [0645] R10
[0646] The air permeability by Gurley method: [0647] 3 seconds/100
mL
Embodiment 12
[0648] The Embodiment 12 was performed in accordance with the
Embodiment 9, except that the deodorizer of zeolite originated from
the natural resources is changed to the deodorizer of the following
synthetic sepiolite to obtain the highly air-permeable and
water-resistance sheet according to the present invention.
[0649] (The Deodorizer of Ultra Fine White Clay)
[0650] Chemical name: [0651] Sepiolite [0652] (Kusumoto Chemical
Ltd., Product Name: Pansil)
[0653] Composition: [0654] SiO.sub.2 (60.5%), MgO (23.8%),
Al.sub.2O.sub.3 (2.4%)
[0655] Particle size: [0656] 5 .mu.m or lower of 88.3% of the
Sepiolite
[0657] Outer structure: [0658] Fine fiber bundle
[0659] Ignition loss: [0660] 11.3% (1000.degree. C.)
[0661] BET surface area: [0662] 270 m.sup.2/g
[0663] The result for the property of the highly air-permeable and
water-resistance sheet is shown as follows.
[0664] The weight of SMS non-woven fabric: [0665] 15 g/m.sup.2
[0666] The weight of MFC: [0667] 5 g/m.sup.2
[0668] The coating amount of the deodorizer [0669] 2.0
g/m.sup.2
[0670] The coating amount of the water repellant layer [0671] 2.0
g/m.sup.2
[0672] The water repellency (JIS P8137): [0673] R10
[0674] The air permeability by Gurley method: [0675] 8 seconds/100
mL
Embodiment 13
[0676] The Embodiment 13 was performed in accordance with the
Embodiment 9, except that the deodorizer of zeolite originated from
the natural resources is changed to the deodorizer of the following
synthetic clay to obtain the highly air-permeable and
water-resistance sheet according to the present invention.
[0677] (The Deodorizer of Synthetic Clay)
[0678] Chemical name: [0679] Clay synthesized from silica, alumina
and metal oxides
[0680] Apparent density: [0681] 0.2 to 0.4
[0682] Particle size: [0683] 10% or lower
[0684] BET surface area: [0685] 250 m.sup.2/g or higher
[0686] pH: 8.5 to 10.0 (JIS-K-1474)
[0687] The result for the property of the highly air-permeable and
water-resistance sheet is shown as follows.
[0688] The weight of SMS non-woven fabric: [0689] 15 g/m.sup.2
[0690] The weight of MFC: [0691] 5 g/m.sup.2
[0692] The coating amount of the deodorizer [0693] 2.05
g/m.sup.2
[0694] The coating amount of the water repellant layer [0695] 2.05
g/m.sup.2
[0696] The water repellency (JIS P8137): [0697] R10
[0698] The air permeability by Gurley method: [0699] 3 seconds/100
mL
Embodiment 14
[0700] The Embodiment 14 was performed in accordance with the
Embodiment 9, except that the deodorizer of zeolite originated from
the natural resources is changed to the deodorizer of the following
zeolite supporting silver to obtain the highly air-permeable and
water-resistance sheet according to the present invention.
[0701] (The Deodorizer of Zeolite Supporting Silver)
[0702] Substance name: [0703] zeolite supporting silver [0704]
(Sinanen Zeomic Co. Ltd., Product name: Zeomic HW10N)
[0705] Structural formula:
Ag.sub.2OAl.sub.2O.sub.3xSiO.sub.2yH.sub.2O, x=2, y=0.about.1
[0706] Particle size: [0707] 0.6 to 2.5 .mu.m
[0708] Apparent density: [0709] 0.4
[0710] Absolute specific gravity: [0711] 2.1
[0712] Pore size: [0713] 3 to 10.degree.
[0714] BET surface area: [0715] 600 m.sup.2/g
[0716] Specific heat: [0717] 0.26 Cal/g
[0718] pH: 7 to 9 (JIS-K-1474)
[0719] The result for the property of the highly air-permeable and
water-resistance sheet is shown as follow.
[0720] The weight of SMS non-woven fabric: [0721] 15 g/m.sup.2
[0722] The weight of MFC: [0723] 5 g/m.sup.2
[0724] The coating amount of the deodorizer [0725] 2.0
g/m.sup.2
[0726] The coating amount of the water repellant layer [0727] 2.0
g/m.sup.2
[0728] The water repellency (JIS P8137): [0729] R10
[0730] The air permeability by Gurley method: [0731] 2 seconds/100
mL
Embodiment 15
[0732] The Embodiment 15 was performed in accordance with the
Embodiment 9, except that the deodorizer of zeolite originated from
the natural resources is changed to the deodorizer of the following
synthetic zeolite to obtain the highly air-permeable and
water-resistance sheet according to the present invention.
[0733] (The Deodorizer of Synthetic Zeolite)
[0734] Substance name: [0735] zeolite [0736] (Asahi Glass Co. Ltd.,
Product Name: Zeolite)
[0737] Structural formula:
NaO.sub.2Al.sub.2O.sub.32SiO.sub.2nH.sub.2O
[0738] Particle size: [0739] 3.0 .mu.m
[0740] Apparent density: [0741] 0.36
[0742] Ignition loss: [0743] 18.5% (800.degree. C.)
[0744] pH: 11.8 (JIS-K-1474)
[0745] The result for the property of the highly air-permeable and
water-resistance sheet is shown as follow.
[0746] The weight of SMS non-woven fabric: [0747] 15 g/m.sup.2
[0748] The weight of MFC: [0749] 5 g/m.sup.2
[0750] The coating amount of the deodorizer [0751] 2.1
g/m.sup.2
[0752] The coating amount of the water repellant layer [0753] 2.1
g/m.sup.2
[0754] The water repellency (JIS P8137): [0755] R10
[0756] The air permeability by Gurley method: [0757] 2 seconds/100
mL
Embodiment 16
[0758] The Embodiment 16 was performed in accordance with the
Embodiment 9, except that the deodorizer of zeolite originated from
the natural resources is changed to the deodorizer of the following
metal oxide, and the condition thereof is changed to the following
condition for manufacturing it to obtain the highly air-permeable
and water-resistance sheet according to the present invention. In
the Embodiment, since low concentration of the suspended liquid is
used for the deodorizer, the concentration of the solid content in
the mixed coating composition of the deodorizer and the water
repellant layer is changed from 40 weight % in the Embodiment 9 to
35 weight %, and the line diameter of the bar is changed from 0.15
mm to 0.20 mm so as to adjust the coating amount.
[0759] (The Deodorizer of Metal Oxide)
[0760] Substance name: [0761] metal oxide deodorizer [0762] (Daiwa
chemical industry Co. Ltd., Product name: Zaobatac PSG)
[0763] Appearance [0764] suspended liquid having milk white
color
[0765] Concentration of the solid content [0766] 3.0 weight %
[0767] Ionic character: [0768] Anion
[0769] Safety: [0770] Acute oral toxicity LD50 20,000 mg/kg or
more
[0771] Dermal irritancy: [0772] Japanese Society for Cutaneous
Health: Pass
[0773] The result for the property of the highly air-permeable and
water-resistance sheet is shown as follow.
[0774] The weight of SMS non-woven fabric: [0775] 15 g/m.sup.2
[0776] The weight of MFC: [0777] 5 g/m.sup.2
[0778] The coating amount of the deodorizer [0779] 2.05
g/m.sup.2
[0780] The coating amount of the water repellant layer [0781] 2.05
g/m.sup.2
[0782] The water repellency (JIS P8137): [0783] R10
[0784] The air permeability by Gurley method: [0785] 3 seconds/100
mL
Embodiment 17
[0786] The Embodiment 17 was performed in accordance with the
Embodiment 9, except that the deodorizer and water repellant layer
of the Embodiment 9, a mixing ratio of the deodorizer and water
repellant layer, line diameter of the bar are changed as Table 8,
and the coating amount of the water repellant layer is constantly 2
g, and the coating amount of the deodorizer is changed to double
volume as used in the Embodiment 9 to obtain the highly
air-permeable and water-resistance sheet according to the present
invention.
Embodiment 18
[0787] The Embodiment 18 was performed in accordance with the
Embodiment 9, except that a mixing ratio of the deodorizer and
water repellant layer, line diameter of the bar are changed as
Table 8, and the coating amount of the water repellant layer is
constantly 2 g, and the coating amount of the deodorizer is changed
to double volume as used in the Embodiment 9 to obtain the highly
air-permeable and water-resistance sheet according to the present
invention.
[0788] Coating date and the property of the Coating data of the
property of the highly air-permeable and water-resistance sheet as
manufactured in the Embodiments 17 and 18 are shown in Table 8. It
should be noted that the property of the coating data and the
physicality are collectively described in Table 8.
TABLE-US-00008 TABLE 8 Embodiment Embodiment Embodiment 9 17 18
Ratio of deodorant 1 2 3 Ratio of 1 1 1 water repellant Linear
diameter 0.15 0.20 0.25 of the bar (mm) Coating amount of 2.05 4.13
6.22 deodorant (g/m.sup.2) Coating amount of 2.05 2.07 2.08 water
repellant (g/m.sup.2) Total coating 4.1 6.2 8.3 amount (g/m.sup.2)
Water repellency 10 10 10 (JIS P 8137) Air permeability 2 6 5
(s/100 mL) (JIS P8117)
Comparative Example 6
[0789] The composite sheet as obtained in the Embodiment 9 was used
as a sheet for comparison. The sheet for comparison was not
subjected to the heat press treatment, and was not coated with the
water repellant layer and the deodorizer.
Comparative Example 7
[0790] The comparative example 7 was performed in accordance with
the Embodiment 9, except that the deodorizer is not used, and it
was coated to the composite sheet using the coating composition
only containing the following water repellant layer to obtain a
sheet for comparison.
[0791] <Preparation of the Coating Composition for the Water
Repellant Layer>
[0792] 50 weight parts of the olefinic water repellent (Meisei
Chemical Works Ltd., Product name: Petrox P300) and 48 weight parts
of stylene butadiene resin (Nippon A&L Inc., Product name:
Smartex PA3802) were mixed under stirring to prepare a main agent.
Then, prior to performing the coating, 2 weight parts of zirconium
carbonate cross linker (Nippon Light Metal Co. Ltd., Product name:
Bay coat 20) was added to the main agent, and water was added to
prepare the coating composition having 40 weight % of the solid
content. At that time, the viscosity of the coating composition was
95 mPas, and was 17 seconds in accordance with Zahn cup method.
[0793] <Preparation of the Sheet by the Coating of the Coating
Composition of the Water Repellant Layer>
[0794] The above-mentioned coating composition for the water
repellant layer was coated to the side of the fine fibrous-form
cellulose of the composite sheet as obtained in the Embodiment 9
with the flexographic coater in accordance with the following
condition. The coating amount was 2.3 g/m.sup.2.
[0795] Aniolox roll: [0796] 130 lines
[0797] Coating speed: [0798] 100 g/minute
[0799] Dry temperature of the air drier: [0800] 100.degree. C.
[0801] After the coating, the heat press treatment was performed
(linear pressure: 100 kg/cm). Then, it was processed at 120.degree.
C. for 30 minutes in the drier to prepare the sheet.
Comparative Example 8
[0802] The backsheet which is used in the commercially available
diaper (Unicharm Co. Ltd., Product name: Muni Oshiri Pure),
comprising the air permeable film in which CaCO.sub.3 is added was
used as a sheet for comparison.
[0803] Next, the following examination was performed with regard to
the sheets as prepared in the Embodiments 9 to 18 and the
Comparative examples 6 to 8.
[0804] [Air Permeability and Smoothness Before and after the Heat
Press Treatment]
[0805] With regard to the sheets of the Embodiments 9 to 18 and the
Comparative example 7 during the manufacturing process performing
the heat press treatment, the air permeability and smoothness
before and after the heat press treatment were measured using
Gurley densometer (JIS P8117) and Bekk smoothness tester (JIS
P8119), respectively. The result is shown in Table 9. It should be
noted that with regard to the Comparative examples 6 and 8, the air
permeability and smoothness as measured above was shown in Table 9
as the values before the heat press treatment.
[0806] As clearly shown in Table 9, with regard to the highly
air-permeable and water-resistance sheet according to the present
invention (the Embodiments 9 to 18), it was confirmed that the
printing capacity was improved due to the increase of the
smoothness by the heat press treatment and the air permeability
value which relates to the air permeability was increased. It
should be noted that the sheets can be practically applicable even
though the air permeability is increased such as.
TABLE-US-00009 TABLE 9 Before After heat press treatment heat press
treatment Air Smooth- Air Smooth- permeability ness permeability
ness (s/100 mL) (s) (s/100 mL) (s) Embodiment 9 2 6 10 41
Embodiment 10 6 6 10 21 Embodiment 11 3 6 5 20 Embodiment 12 8 6 73
84 Embodiment 13 3 8 29 51 Embodiment 14 2 6 11 30 Embodiment 15 2
8 10 45 Embodiment 16 3 4 33 70 Embodiment 17 6 6 30 67 Embodiment
18 5 4 36 106 Comparative 1 2 -- -- example 6 Comparative 2 5 6 31
example 7 Comparative 150 24 -- -- example 8
[0807] [Water Resistance]
[0808] The water resistance of the sheets as obtained in the
Embodiments 9 to 18 and the Comparative examples 6 and 8 was
confirmed with the following method. That is, the sheet was
disposed on the paper filter, 10 wiper papers (Crecia Co. Ltd.,
Product name: Kim Towel) containing enough amounts of water were
disposed on the sheet, and 5 kg of the weight was further disposed
thereon, and the leaked water to the paper filter was observed.
[0809] As the result, in the Embodiments 9 to 18 and the
Comparative example 7 and 8, any leakages to the filter paper were
not observed after 5 hours, and the water resistance was extremely
good. On the other hand, in the Comparative example 6, the water
leakage was occurred after 1 minute, and it has less water
resistance. The condition of the water resistance test is harder
than the use condition of the backsheet for the commercially
available child diaper. So, even though the highly air-permeable
and water-resistance sheet according to the present invention
(Embodiments 9 and 18) is used for the backsheet of the
commercially available child diaper, there is no risk of the
leakage for long time, and it can stand the practical use.
[0810] In addition, with regard to the sheet of the Embodiments 9
to 18 and the Comparative examples 6 to 8, the following deodorant
property 1 using ammonium was examined. The result is shown in
Table 10.
TABLE-US-00010 TABLE 10 Ammonium concentration (ppm) 10 20 40 60 80
100 120 min min min min min min min Embodiment 9 86 40 36 30 21 17
16 Embodiment 10 90 43 35 28 25 18 18 Embodiment 11 88 45 32 27 23
21 21 Embodiment 12 90 57 48 41 33 29 28 Embodiment 13 82 40 31 25
21 18 18 Embodiment 14 82 36 30 22 21 20 18 Embodiment 15 91 62 47
39 32 27 26 Embodiment 16 63 40 28 25 21 18 16 Embodiment 17 78 38
32 25 20 16 15 Embodiment 18 70 35 28 21 16 12 10 Comparative 95 90
88 86 86 85 85 example 6 Comparative 94 90 87 87 85 85 83 example 7
Comparative 92 78 58 50 43 40 38 example 8
[0811] As clearly shown in Table 10, in the highly air-permeable
and water-resistance sheet according to the present invention using
the deodorizer (the Embodiments 9 to 18), the ammonium
concentration was gradually decreased in progress of the time, in
comparison with the Comparative examples 6 and 7 not using the
deodorizer. The effect of the deodorization was observed. With
regard to the Comparative example 8, calcium carbonate which is
added to the porous film has some deodorization effect.
Accordingly, the ammonium concentration was gradually decreased
among the Comparative examples.
[0812] In addition, with regard to the sheets of the Embodiments 9
to 11 and the Comparative example 8, the following deodorant
property 2 using ammonium was examined. The result is shown in
Table 11.
TABLE-US-00011 TABLE 11 Ammonium concentration (ppm) 10 20 30 40 60
80 min min min min min min Embodiment 9 40 60 76 89 108 118
Embodiment 10 29 49 66 74 96 105 Embodiment 11 25 45 61 70 90 103
Comparative 41 65 91 110 127 134 example 8
[0813] As clearly shown in Table 11, it was confirmed that the
increase of the amount of the deodorizer in the sheet will lead to
the less amount of ammonium to be leaked. It was found that the
leaked ammonium amount is greatly low in comparison with the film
of the Comparative example 8 having low air permeability.
Embodiment 19
[0814] An example will be described to confirm that the highly
air-permeable and water-resistance sheet as obtained in the
Embodiment 9 can be applied to the backsheet of the child diaper.
The backsheet of the commercially available child diaper was
replaced with the highly air-permeable and water-resistance sheet
according to the present invention to manufacture a diaper for
test. The wearing test was performed using the diaper for test to
the baby. As the test, the urine leakage, the skin to be stuffy and
the rush were observed after the predetermined period was passed
from the beginning of wearing.
[0815] <Preparation of the Diaper for Test>
[0816] The backsheet (laminate of the air permeable film and the
non-woven fabric) was removed from the child diaper as shown in
FIGS. 12 and 13 (Unicham Co. Ltd., Product name: Muni Nobi-ru fit)
by cold spraying the connecting part. The highly air-permeable and
water-resistance sheet according to the present invention was
disposed in the removed part of the diaper to prepare 40 of the
child diapers for test.
[0817] <The Wearing Test by Baby>
[0818] 40 of the child diapers for test were prepared, and it was
worn to 8 babies (4 male babies, and 4 girl babies) having normal
excretion mechanism (5 diapers per baby used). The parent of the
wearer was asked to recode dairy report indicating its use, all of
the diapers after use were retrieved, and the leakage from the
disposed highly air-permeable and water-resistance sheet according
to the present invention was confirmed. The wearing time was set
for 3 hours in average. As the result, any leakages from the
disposed highly air-permeable and water-resistance sheet according
to the present invention were not observed in 37 diapers among 40
diapers. In addition, the bleeding in the circular form was
observed at the rear part of the diaper was observed in 3 diapers,
and the bleeding in the pinhole form was observed in 2 diapers.
With regard to 3 diapers among 40 diapers, the leakage of feces and
urine was observed in 1 diaper, respectively. In addition, with
regard to all of babies, there is no stuffy and rush. In addition,
it was not reported from the parent that any smells from the
excretions such as urine and feces during wearing is occurred. It
was confirmed from these results that the child diaper in which the
highly air-permeable and water-resistance sheet according to the
present invention is used for the backsheet can be practically
applicable.
[0819] [Absorptive and Desorptive Amount to be Defined]
[0820] The absorptive amount to be defined was measured in
accordance with "Method for examining absorptive amount of high
absorptive resin" as stated in JIS K7223-1996. In addition, the
desorptive amount to be defined was estimated in which after the
absorptive amount to be designed was measured, water was desorbed
by centrifugation at 1000.times.g for 10 minutes.
[0821] [Water Pressure Resistance]
[0822] The water pressure resistance was examined in accordance
with the following method.
[0823] FIG. 18 shows a schematic view of an apparatus for examining
water resistance, wherein (a) indicates an overall view thereof,
and (b) indicates an enlarged view of the sample applied portion in
the apparatus.
[0824] The sample size is set at 5 cm.times.5 cm, and the sample is
disposed as follows.
[0825] 1) Layer 2 filter papers 303 (Type: No. 2, Size: 15
cm.times.15 cm, hereinafter, the same applied) to a glass plate 302
on a jack 301.
[0826] 2) Place a sample 304 to be measure such that the coat
surface of SAP faces in the perpendicular direction on the center
of a filter paper 303.
[0827] 3) Place a tissue paper 305 on the sample 304, wherein the
tissue paper 305 has a size smaller than the sample 304.
[0828] 4) Next, place an acrylic pipe 306 as follows.
[0829] 5) Attach a packing 308 for cushioning at adjusting the hole
on the bottom surface of an acrylic mounter 307 integrating with
the acrylic pipe 306.
[0830] 6) Dispose the acrylic pipe 306 such that the hole of the
bottom side of the acrylic pipe 306 is matched to the center of the
sample 304 by means of holding the acrylic pipe 306 with a clamp
310 of a stand 309. At this time, the acrylic pipe 306 is held such
that it is in the vertical direction of the sample 304.
[0831] 7) After the acrylic pipe 306 is positioned, fix the
position of the acrylic pipe 306 by closing the clamp 310.
[0832] 8) Raise a jack 301, and Close not so as to leak the liquid
through the packing 308 for cushioning between the glass plate 302
and the acrylic mounter 307 of the under side of the acrylic pipe
306.
[0833] Next, the water pressure resistance was measured to examine
the water resistance.
[0834] First, small amount (e.g. 2 to 3 mL) of a measuring liquid
(0.9% NaCl aqueous solution, colored with Food Blue No. 1)
contained in washing bottle is gently introduced from the upper end
of the acrylic pipe 306. In this case, it is confirmed that the
sample surface absorbs enough liquid.
[0835] After the state is maintained for 1 minute, the SAP particle
of the sample surface is swelled. Also in this case, it is
confirmed that the measuring liquid is not leaked.
[0836] Next, a funnel 312 is mounted on the upper end of the
acrylic pipe 306, and the wearing liquid is introduced from the
funnel 312. The scale of the acrylic pipe is read at occurring the
liquid leakage to the filter paper on the glass plate, the scale is
assigned as water pressure resistance (P). The read was every 10
mmH.sub.2O.
[0837] It should be noted that this examination is performed while
it was appropriately monitored with a mirror 313 disposed under the
glass plate 302.
[0838] [The Hydration Capacity]
[0839] The hydration capacity is aimed to compare the dispersive
stability, and the method for measuring the same is preferably easy
and stable. Therefore, in the present invention, the hydrating
capacity means a volume of precipitated MFC by centrifugation.
Hereinafter, the method for measuring will be indicated.
[0840] The cellulose fiber (0.5 g) to be subjected in 50 mL of
water dispersion liquid was taken in the centrifuging tube (inner
diameter 30 mm.times.length 100 mm, volume 50 mL), and the tube was
centrifuged at 2000.times.g (3300 rpm) for 10 minutes to read the
precipitated volume (mL), thereby calculating the hydration
capacity in accordance with the following formula.
The hydration capacity (mL/g)=Precipitated volume (mL)/Weigh of
Cellulose fiber (g)
[0841] [Air Permeability]
[0842] 1. Measurement of Air Permeability by Gurley Method
[0843] The measurement was performed in accordance with the method
of JIS-P8117. That is, the highly air-permeable and
water-resistance sheet according to the present invention is cut
into it having 645 cm2 of the area. The air permeability was
measured using No. 323 Gurley Type Densometer made by Yasuda Seiki
Seisakusho Ltd., in that a time (second) which 100 mL of air is
passed is measure by timer.
[0844] 2. Measurement of Water Vapor Transmission Rate (WVT) by the
Cup Method
[0845] The measurement was performed in accordance with JIS Z0208
(ASTM E-96). [0846] Sample to be tested
[0847] The highly air-permeable and water-resistance sheet
according to the present invention is cut in the circular form
having 75 mm of diameter. [0848] Condition
[0849] 40.degree. C., relative humidity 90.+-.2% [0850] The sample
to be tested was mounted to the cup, the circumference thereof was
sealed, and the moisture is adsorbed under high temperature and
humidity for a predetermined time. The wetted weight corresponding
to 24 hours was estimated by means of the average increased amount
at the steady state of the weight increase and by means of the
weight increasing curve against time at the linear portion of the
curve. [0851] It was estimated in accordance with the following
formula.
[0851] WVT=(G/t)/A(g/m.sup.2,24 hours)
[0852] G: Change in weight
[0853] t: time (time)
[0854] A: Area of test (area of the cup portion) (m)
[0855] [Method for Measuring of Table 5]
[0856] Thickness: JIS P8118
[0857] Air permeability with Gurley method: JIS P8117
[0858] Smoothness: JIS P8119
[0859] [Deodorant Property 1 Using Ammonium]
[0860] The deodorant property 1 using ammonium was examined using
apparatus of FIG. 19 in accordance with the following method. The
sheets in the Embodiment 9 to 18 and the sheets of the Comparative
examples 7 and 8 were used as the following were used as a sample
for (1).
[0861] (1) Set the sample (50.times.50 mm) to the bottom of 1.80 of
sealed Glass bottle
[0862] (2) Introduce the sample into glass fiber filter paper such
that the concentration of the ammonium in the sealed bottle is 100
ppm.
[0863] (3) After ammonium was introduced, quantify the
concentrations of the ammonium gas remained in the bottle at 10,
20, 40, 60, 80, 100 and 120 minutes by means of opening the cock,
introducing the ammonium from the entrance of the glass pipe to the
gas detector connected with ammonium detector tube.
[0864] [Deodorant Property 2 Using Ammonium]
[0865] The Deodorant property 2 using ammonium was measured using
the apparatus of FIG. 20 in accordance with the following method.
As the following (2), the sheets of the Embodiments 9 to 11 and the
Comparative example 8 were used.
[0866] (1) Prepare 2 cups made with polypropylene having 60 mm of
diameter at the bottom, 90 mm of diameter at the upper surface, and
125 mm of the height (volume 500 mL).
[0867] (2) Next, introduce 250 ppm of ammonium into the 2 cups, and
cover the inlet (upper surface) of the cup with the sample (sheet),
as shown in FIG. 20.
[0868] (3) Dispose the 2 cups equipped with the sample and
introduced the ammonium water into cubic ammonium gas saturation
room having acrylate resin box having 0.015 m.sup.3, and then
qualify and recode the ammonium concentration to be leaked and/or
created from the cup.
[0869] As mentioned above, the present invention has been described
with reference to the preferred embodiment. Here, although the
present invention has been explained by indicating particular
examples, it is obvious that any modification and change to these
examples can be made without departing from the spirit and scope of
the present invention defined in the Claims. That is, it should not
be interpreted that the present invention is limited to the
detailed example and drawing as attached.
INDUSTRIALLY APPLICABILITY
[0870] The highly air-permeable and water-resistance sheet
according to the present invention has a superior in dust
resistance and bacteria barrier. The present invention is
advantageously applicable to a use in which such a nature is taken
into confidence, such as hygiene product, medical product, surgical
product, distilled packaging product, battery separator, and fine
printing material.
* * * * *